17-73775017-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73775017
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 73775017
    reference: chr 17
allele count: 1
allele frequency: 8.288437629506838e-6
allele num: 120650
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000468484
  ensembl transcript: ENST00000587171
  gene symbol: H3F3B
  hgvsc: ENST00000587171.1:c.156T>A
  hgvsp: ENST00000587171.1:c.156T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000465403
  ensembl transcript: ENST00000586270
  gene symbol: H3F3B
  hgvsc: ENST00000586270.1:c.156T>A
  hgvsp: ENST00000586270.1:c.156T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000468714
  ensembl transcript: ENST00000587560
  gene symbol: H3F3B
  hgvsc: ENST00000587560.1:c.156T>A
  hgvsp: ENST00000587560.1:c.156T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000466020
  ensembl transcript: ENST00000586607
  gene symbol: H3F3B
  hgvsc: ENST00000586607.1:c.156T>A
  hgvsp: ENST00000586607.1:c.156T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000589949
  gene symbol: H3F3B
  hgvsc: ENST00000589949.1:n.359T>A
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000466663
  ensembl transcript: ENST00000591890
  gene symbol: H3F3B
  hgvsc: ENST00000591890.1:c.156T>A
  hgvsp: ENST00000591890.1:c.156T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000254810
  ensembl transcript: ENST00000254810
  gene symbol: H3F3B
  hgvsc: ENST00000254810.4:c.156T>A
  hgvsp: ENST00000254810.4:c.156T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000467165
  ensembl transcript: ENST00000592643
  gene symbol: H3F3B
  hgvsc: ENST00000592643.1:c.156T>A
  hgvsp: ENST00000592643.1:c.156T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000465813
  ensembl transcript: ENST00000589599
  gene symbol: H3F3B
  hgvsc: ENST00000589599.1:c.156T>A
  hgvsp: ENST00000589599.1:c.156T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000589417
  gene symbol: H3F3B
  hgvsc: ENST00000589417.1:n.372T>A
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000586518
  gene symbol: H3F3B
  hgvsc: ENST00000586518.1:n.837T>A
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000593254
  gene symbol: H3F3B
  hgvsc: ENST00000593254.1:n.118-54T>A
  variant of: http://identifiers.org/hgnc/4765
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 31373
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2362
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11543
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12891
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 604
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 681
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile52Ile
num of homozygotes: 0
population: East Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: South Asian
population: African
reference allele: A
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD

17-73775032-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73775032
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 73775032
    reference: chr 17
allele count: 1
allele frequency: 8.302337938363443e-6
allele num: 120448
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000465813
  ensembl transcript: ENST00000589599
  gene symbol: H3F3B
  hgvsc: ENST00000589599.1:c.141G>A
  hgvsp: ENST00000589599.1:c.141G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000468484
  ensembl transcript: ENST00000587171
  gene symbol: H3F3B
  hgvsc: ENST00000587171.1:c.141G>A
  hgvsp: ENST00000587171.1:c.141G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000468714
  ensembl transcript: ENST00000587560
  gene symbol: H3F3B
  hgvsc: ENST00000587560.1:c.141G>A
  hgvsp: ENST00000587560.1:c.141G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000589949
  gene symbol: H3F3B
  hgvsc: ENST00000589949.1:n.344G>A
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000589417
  gene symbol: H3F3B
  hgvsc: ENST00000589417.1:n.357G>A
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000467165
  ensembl transcript: ENST00000592643
  gene symbol: H3F3B
  hgvsc: ENST00000592643.1:c.141G>A
  hgvsp: ENST00000592643.1:c.141G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000465403
  ensembl transcript: ENST00000586270
  gene symbol: H3F3B
  hgvsc: ENST00000586270.1:c.141G>A
  hgvsp: ENST00000586270.1:c.141G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000466663
  ensembl transcript: ENST00000591890
  gene symbol: H3F3B
  hgvsc: ENST00000591890.1:c.141G>A
  hgvsp: ENST00000591890.1:c.141G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000466020
  ensembl transcript: ENST00000586607
  gene symbol: H3F3B
  hgvsc: ENST00000586607.1:c.141G>A
  hgvsp: ENST00000586607.1:c.141G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000593254
  gene symbol: H3F3B
  hgvsc: ENST00000593254.1:n.118-69G>A
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000254810
  ensembl transcript: ENST00000254810
  gene symbol: H3F3B
  hgvsc: ENST00000254810.4:c.141G>A
  hgvsp: ENST00000254810.4:c.141G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000586518
  gene symbol: H3F3B
  hgvsc: ENST00000586518.1:n.822G>A
  variant of: http://identifiers.org/hgnc/4765
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12790
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 675
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 771
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 482
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 399
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31161
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2333
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val47Val
num of homozygotes: 0
population: East Asian
population: African
population: South Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: ClippingRankSum

17-73775043-GCCTGCAGCGAGCAGGGGAGGAGTGAGCGGACGCTGCCGCACAAAGCCGGCCACCGCCGGGCCATTGTTCCCCCGCCCGACCTA-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73775043
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 73774960
    reference: chr 17
allele count: 1
allele frequency: 8.320159747067144e-6
allele num: 120190
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: splice_donor_variant
  consequence: coding_sequence_variant
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000466020
  ensembl transcript: ENST00000586607
  gene symbol: H3F3B
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000589949
  gene symbol: H3F3B
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: splice_donor_variant
  consequence: coding_sequence_variant
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000465403
  ensembl transcript: ENST00000586270
  gene symbol: H3F3B
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000586518
  gene symbol: H3F3B
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000589417
  gene symbol: H3F3B
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: true
  consequence: splice_acceptor_variant
  consequence: splice_donor_variant
  consequence: coding_sequence_variant
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000254810
  ensembl transcript: ENST00000254810
  gene symbol: H3F3B
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: splice_donor_variant
  consequence: coding_sequence_variant
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000467165
  ensembl transcript: ENST00000592643
  gene symbol: H3F3B
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: splice_donor_variant
  consequence: coding_sequence_variant
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000466663
  ensembl transcript: ENST00000591890
  gene symbol: H3F3B
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: splice_donor_variant
  consequence: coding_sequence_variant
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000465813
  ensembl transcript: ENST00000589599
  gene symbol: H3F3B
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: splice_donor_variant
  consequence: coding_sequence_variant
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000468714
  ensembl transcript: ENST00000587560
  gene symbol: H3F3B
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000593254
  gene symbol: H3F3B
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: splice_donor_variant
  consequence: coding_sequence_variant
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000468484
  ensembl transcript: ENST00000587171
  gene symbol: H3F3B
  variant of: http://identifiers.org/hgnc/4765
canonical: true
consequence: splice acceptor
filter: VQSRTrancheINDEL99.50to99.90
genotype depth: GenotypeDepth
  all individuals: 923
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 663
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11531
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 466
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31045
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: African
population: Latino
population: European (Finnish)
population: East Asian
population: South Asian
population: European (Non-Finnish)
reference allele: GCCTGCAGCGAGCAGGGGAGGAGTGAGCGGACGCTGCCGCACAAAGCCGGCCACCGCCGGGCCATTGTTCCCCCGCCCGACCTA
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD

17-73775052-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73775052
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 73775052
    reference: chr 17
allele count: 1
allele frequency: 8.33152816889674e-6
allele num: 120026
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000589417
  gene symbol: H3F3B
  hgvsc: ENST00000589417.1:n.337C>T
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000468714
  ensembl transcript: ENST00000587560
  gene symbol: H3F3B
  hgvsc: ENST00000587560.1:c.129-8C>T
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000586518
  gene symbol: H3F3B
  hgvsc: ENST00000586518.1:n.802C>T
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000465813
  ensembl transcript: ENST00000589599
  gene symbol: H3F3B
  hgvsc: ENST00000589599.1:c.129-8C>T
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000589949
  gene symbol: H3F3B
  hgvsc: ENST00000589949.1:n.324C>T
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000593254
  gene symbol: H3F3B
  hgvsc: ENST00000593254.1:n.118-89C>T
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000465403
  ensembl transcript: ENST00000586270
  gene symbol: H3F3B
  hgvsc: ENST00000586270.1:c.129-8C>T
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000466663
  ensembl transcript: ENST00000591890
  gene symbol: H3F3B
  hgvsc: ENST00000591890.1:c.129-8C>T
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000466020
  ensembl transcript: ENST00000586607
  gene symbol: H3F3B
  hgvsc: ENST00000586607.1:c.129-8C>T
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000468484
  ensembl transcript: ENST00000587171
  gene symbol: H3F3B
  hgvsc: ENST00000587171.1:c.129-8C>T
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000254810
  ensembl transcript: ENST00000254810
  gene symbol: H3F3B
  hgvsc: ENST00000254810.4:c.129-8C>T
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000467165
  ensembl transcript: ENST00000592643
  gene symbol: H3F3B
  hgvsc: ENST00000592643.1:c.129-8C>T
  variant of: http://identifiers.org/hgnc/4765
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 632
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 588
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30854
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12468
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1181
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11618
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 563
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2202
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.129-8C>T
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: African
population: South Asian
population: Other
population: European (Non-Finnish)
population: East Asian
reference allele: G
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: ClippingRankSum

17-73775054-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73775054
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 73775054
    reference: chr 17
allele count: 2
allele frequency: 1.666139055965611e-5
allele num: 120038
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000467165
  ensembl transcript: ENST00000592643
  gene symbol: H3F3B
  hgvsc: ENST00000592643.1:c.129-10C>T
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000586518
  gene symbol: H3F3B
  hgvsc: ENST00000586518.1:n.800C>T
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000465813
  ensembl transcript: ENST00000589599
  gene symbol: H3F3B
  hgvsc: ENST00000589599.1:c.129-10C>T
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000589417
  gene symbol: H3F3B
  hgvsc: ENST00000589417.1:n.335C>T
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000468484
  ensembl transcript: ENST00000587171
  gene symbol: H3F3B
  hgvsc: ENST00000587171.1:c.129-10C>T
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000468714
  ensembl transcript: ENST00000587560
  gene symbol: H3F3B
  hgvsc: ENST00000587560.1:c.129-10C>T
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000589949
  gene symbol: H3F3B
  hgvsc: ENST00000589949.1:n.322C>T
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000593254
  gene symbol: H3F3B
  hgvsc: ENST00000593254.1:n.118-91C>T
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000254810
  ensembl transcript: ENST00000254810
  gene symbol: H3F3B
  hgvsc: ENST00000254810.4:c.129-10C>T
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000466020
  ensembl transcript: ENST00000586607
  gene symbol: H3F3B
  hgvsc: ENST00000586607.1:c.129-10C>T
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000466663
  ensembl transcript: ENST00000591890
  gene symbol: H3F3B
  hgvsc: ENST00000591890.1:c.129-10C>T
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000465403
  ensembl transcript: ENST00000586270
  gene symbol: H3F3B
  hgvsc: ENST00000586270.1:c.129-10C>T
  variant of: http://identifiers.org/hgnc/4765
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 571
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 629
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 586
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12433
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2197
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30851
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11629
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1209
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Other
population: East Asian
reference allele: G
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: DP
site quality: MQRankSum

17-73775055-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73775055
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 73775055
    reference: chr 17
allele count: 15
allele frequency: 1.25e-4
allele num: 120000
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000254810
  ensembl transcript: ENST00000254810
  gene symbol: H3F3B
  hgvsc: ENST00000254810.4:c.129-11G>C
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000589949
  gene symbol: H3F3B
  hgvsc: ENST00000589949.1:n.321G>C
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000593254
  gene symbol: H3F3B
  hgvsc: ENST00000593254.1:n.118-92G>C
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000466663
  ensembl transcript: ENST00000591890
  gene symbol: H3F3B
  hgvsc: ENST00000591890.1:c.129-11G>C
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000465813
  ensembl transcript: ENST00000589599
  gene symbol: H3F3B
  hgvsc: ENST00000589599.1:c.129-11G>C
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000468714
  ensembl transcript: ENST00000587560
  gene symbol: H3F3B
  hgvsc: ENST00000587560.1:c.129-11G>C
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000586518
  gene symbol: H3F3B
  hgvsc: ENST00000586518.1:n.799G>C
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000467165
  ensembl transcript: ENST00000592643
  gene symbol: H3F3B
  hgvsc: ENST00000592643.1:c.129-11G>C
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000465403
  ensembl transcript: ENST00000586270
  gene symbol: H3F3B
  hgvsc: ENST00000586270.1:c.129-11G>C
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000589417
  gene symbol: H3F3B
  hgvsc: ENST00000589417.1:n.334G>C
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000466020
  ensembl transcript: ENST00000586607
  gene symbol: H3F3B
  hgvsc: ENST00000586607.1:c.129-11G>C
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000468484
  ensembl transcript: ENST00000587171
  gene symbol: H3F3B
  hgvsc: ENST00000587171.1:c.129-11G>C
  variant of: http://identifiers.org/hgnc/4765
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12406
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 30820
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 4.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 578
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11643
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 594
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1239
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2192
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Other
population: Latino
population: East Asian
population: European (Non-Finnish)
population: African
reference allele: C
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum

http://identifiers.org/exac.variant/17-73775056-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73775056
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 73775056
    reference: chr 17
allele count: 2
allele frequency: 1.667278001934042e-5
allele num: 119956
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000468484
  ensembl transcript: ENST00000587171
  gene symbol: H3F3B
  hgvsc: ENST00000587171.1:c.129-12T>G
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000465813
  ensembl transcript: ENST00000589599
  gene symbol: H3F3B
  hgvsc: ENST00000589599.1:c.129-12T>G
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000586518
  gene symbol: H3F3B
  hgvsc: ENST00000586518.1:n.798T>G
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000467165
  ensembl transcript: ENST00000592643
  gene symbol: H3F3B
  hgvsc: ENST00000592643.1:c.129-12T>G
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000589949
  gene symbol: H3F3B
  hgvsc: ENST00000589949.1:n.320T>G
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000465403
  ensembl transcript: ENST00000586270
  gene symbol: H3F3B
  hgvsc: ENST00000586270.1:c.129-12T>G
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000593254
  gene symbol: H3F3B
  hgvsc: ENST00000593254.1:n.118-93T>G
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000466020
  ensembl transcript: ENST00000586607
  gene symbol: H3F3B
  hgvsc: ENST00000586607.1:c.129-12T>G
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000589417
  gene symbol: H3F3B
  hgvsc: ENST00000589417.1:n.333T>G
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000254810
  ensembl transcript: ENST00000254810
  gene symbol: H3F3B
  hgvsc: ENST00000254810.4:c.129-12T>G
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000466663
  ensembl transcript: ENST00000591890
  gene symbol: H3F3B
  hgvsc: ENST00000591890.1:c.129-12T>G
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000468714
  ensembl transcript: ENST00000587560
  gene symbol: H3F3B
  hgvsc: ENST00000587560.1:c.129-12T>G
  variant of: http://identifiers.org/hgnc/4765
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 584
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11651
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 601
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1290
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12387
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30795
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2181
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 624
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: South Asian
population: African
population: Other
population: Latino
population: European (Non-Finnish)
reference allele: A
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum

17-73775057-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73775057
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 73775057
    reference: chr 17
allele count: 145
allele frequency: 1.209199926614073e-3
allele num: 119914
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000589949
  gene symbol: H3F3B
  hgvsc: ENST00000589949.1:n.319C>T
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000468714
  ensembl transcript: ENST00000587560
  gene symbol: H3F3B
  hgvsc: ENST00000587560.1:c.129-13C>T
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000466663
  ensembl transcript: ENST00000591890
  gene symbol: H3F3B
  hgvsc: ENST00000591890.1:c.129-13C>T
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000586518
  gene symbol: H3F3B
  hgvsc: ENST00000586518.1:n.797C>T
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000589417
  gene symbol: H3F3B
  hgvsc: ENST00000589417.1:n.332C>T
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000467165
  ensembl transcript: ENST00000592643
  gene symbol: H3F3B
  hgvsc: ENST00000592643.1:c.129-13C>T
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000465403
  ensembl transcript: ENST00000586270
  gene symbol: H3F3B
  hgvsc: ENST00000586270.1:c.129-13C>T
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000465813
  ensembl transcript: ENST00000589599
  gene symbol: H3F3B
  hgvsc: ENST00000589599.1:c.129-13C>T
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000254810
  ensembl transcript: ENST00000254810
  gene symbol: H3F3B
  hgvsc: ENST00000254810.4:c.129-13C>T
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000466020
  ensembl transcript: ENST00000586607
  gene symbol: H3F3B
  hgvsc: ENST00000586607.1:c.129-13C>T
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000468484
  ensembl transcript: ENST00000587171
  gene symbol: H3F3B
  hgvsc: ENST00000587171.1:c.129-13C>T
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000593254
  gene symbol: H3F3B
  hgvsc: ENST00000593254.1:n.118-94C>T
  variant of: http://identifiers.org/hgnc/4765
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11608
  bin: 2.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 614
  bin: 4.25e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 4.75e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 12370
  bin: 3.25e1
  variant carriers: 24
genotype depth: GenotypeDepth
  all individuals: 2178
  bin: 3.75e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 6.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 650
  bin: 1.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 5.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 5.25e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 1363
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 603
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 6.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 30709
  bin: 2.75e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
num of homozygotes: 1
population: Other
population: Latino
population: South Asian
population: East Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: DP

17-73775057-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73775057
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 73775057
    reference: chr 17
allele count: 12
allele frequency: 1.00071718064613e-4
allele num: 119914
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000589949
  gene symbol: H3F3B
  hgvsc: ENST00000589949.1:n.319C>G
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000465403
  ensembl transcript: ENST00000586270
  gene symbol: H3F3B
  hgvsc: ENST00000586270.1:c.129-13C>G
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000254810
  ensembl transcript: ENST00000254810
  gene symbol: H3F3B
  hgvsc: ENST00000254810.4:c.129-13C>G
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000465813
  ensembl transcript: ENST00000589599
  gene symbol: H3F3B
  hgvsc: ENST00000589599.1:c.129-13C>G
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000468484
  ensembl transcript: ENST00000587171
  gene symbol: H3F3B
  hgvsc: ENST00000587171.1:c.129-13C>G
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000466020
  ensembl transcript: ENST00000586607
  gene symbol: H3F3B
  hgvsc: ENST00000586607.1:c.129-13C>G
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000586518
  gene symbol: H3F3B
  hgvsc: ENST00000586518.1:n.797C>G
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000593254
  gene symbol: H3F3B
  hgvsc: ENST00000593254.1:n.118-94C>G
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000467165
  ensembl transcript: ENST00000592643
  gene symbol: H3F3B
  hgvsc: ENST00000592643.1:c.129-13C>G
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000589417
  gene symbol: H3F3B
  hgvsc: ENST00000589417.1:n.332C>G
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000468714
  ensembl transcript: ENST00000587560
  gene symbol: H3F3B
  hgvsc: ENST00000587560.1:c.129-13C>G
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000466663
  ensembl transcript: ENST00000591890
  gene symbol: H3F3B
  hgvsc: ENST00000591890.1:c.129-13C>G
  variant of: http://identifiers.org/hgnc/4765
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 614
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11608
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12370
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 30709
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1363
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 603
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 650
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2178
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: African
population: Latino
population: South Asian
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ

17-73775058-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73775058
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 73775058
    reference: chr 17
allele count: 1
allele frequency: 8.339170752860335e-6
allele num: 119916
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000254810
  ensembl transcript: ENST00000254810
  gene symbol: H3F3B
  hgvsc: ENST00000254810.4:c.129-14C>G
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000468714
  ensembl transcript: ENST00000587560
  gene symbol: H3F3B
  hgvsc: ENST00000587560.1:c.129-14C>G
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000465403
  ensembl transcript: ENST00000586270
  gene symbol: H3F3B
  hgvsc: ENST00000586270.1:c.129-14C>G
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000593254
  gene symbol: H3F3B
  hgvsc: ENST00000593254.1:n.118-95C>G
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000467165
  ensembl transcript: ENST00000592643
  gene symbol: H3F3B
  hgvsc: ENST00000592643.1:c.129-14C>G
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000466020
  ensembl transcript: ENST00000586607
  gene symbol: H3F3B
  hgvsc: ENST00000586607.1:c.129-14C>G
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000589417
  gene symbol: H3F3B
  hgvsc: ENST00000589417.1:n.331C>G
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000465813
  ensembl transcript: ENST00000589599
  gene symbol: H3F3B
  hgvsc: ENST00000589599.1:c.129-14C>G
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000468484
  ensembl transcript: ENST00000587171
  gene symbol: H3F3B
  hgvsc: ENST00000587171.1:c.129-14C>G
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000466663
  ensembl transcript: ENST00000591890
  gene symbol: H3F3B
  hgvsc: ENST00000591890.1:c.129-14C>G
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000586518
  gene symbol: H3F3B
  hgvsc: ENST00000586518.1:n.796C>G
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000589949
  gene symbol: H3F3B
  hgvsc: ENST00000589949.1:n.318C>G
  variant of: http://identifiers.org/hgnc/4765
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2158
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 627
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 606
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1367
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12349
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11653
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 609
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30800
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Latino
population: Other
reference allele: G
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: QD

17-73775059-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73775059
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 73775059
    reference: chr 17
allele count: 3
allele frequency: 2.503463123988184e-5
allele num: 119834
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000466663
  ensembl transcript: ENST00000591890
  gene symbol: H3F3B
  hgvsc: ENST00000591890.1:c.129-15C>T
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000254810
  ensembl transcript: ENST00000254810
  gene symbol: H3F3B
  hgvsc: ENST00000254810.4:c.129-15C>T
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000589417
  gene symbol: H3F3B
  hgvsc: ENST00000589417.1:n.330C>T
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000467165
  ensembl transcript: ENST00000592643
  gene symbol: H3F3B
  hgvsc: ENST00000592643.1:c.129-15C>T
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000589949
  gene symbol: H3F3B
  hgvsc: ENST00000589949.1:n.317C>T
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000465403
  ensembl transcript: ENST00000586270
  gene symbol: H3F3B
  hgvsc: ENST00000586270.1:c.129-15C>T
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000465813
  ensembl transcript: ENST00000589599
  gene symbol: H3F3B
  hgvsc: ENST00000589599.1:c.129-15C>T
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000466020
  ensembl transcript: ENST00000586607
  gene symbol: H3F3B
  hgvsc: ENST00000586607.1:c.129-15C>T
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000586518
  gene symbol: H3F3B
  hgvsc: ENST00000586518.1:n.795C>T
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000468484
  ensembl transcript: ENST00000587171
  gene symbol: H3F3B
  hgvsc: ENST00000587171.1:c.129-15C>T
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000593254
  gene symbol: H3F3B
  hgvsc: ENST00000593254.1:n.118-96C>T
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000468714
  ensembl transcript: ENST00000587560
  gene symbol: H3F3B
  hgvsc: ENST00000587560.1:c.129-15C>T
  variant of: http://identifiers.org/hgnc/4765
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 698
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2154
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 627
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11609
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1491
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12296
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30687
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: African
population: Latino
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: QD

17-73775060-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73775060
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 73775060
    reference: chr 17
allele count: 6
allele frequency: 5.006257822277847e-5
allele num: 119850
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000593254
  gene symbol: H3F3B
  hgvsc: ENST00000593254.1:n.118-97C>T
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000466020
  ensembl transcript: ENST00000586607
  gene symbol: H3F3B
  hgvsc: ENST00000586607.1:c.129-16C>T
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000586518
  gene symbol: H3F3B
  hgvsc: ENST00000586518.1:n.794C>T
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000468484
  ensembl transcript: ENST00000587171
  gene symbol: H3F3B
  hgvsc: ENST00000587171.1:c.129-16C>T
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000589417
  gene symbol: H3F3B
  hgvsc: ENST00000589417.1:n.329C>T
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000467165
  ensembl transcript: ENST00000592643
  gene symbol: H3F3B
  hgvsc: ENST00000592643.1:c.129-16C>T
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000465403
  ensembl transcript: ENST00000586270
  gene symbol: H3F3B
  hgvsc: ENST00000586270.1:c.129-16C>T
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000466663
  ensembl transcript: ENST00000591890
  gene symbol: H3F3B
  hgvsc: ENST00000591890.1:c.129-16C>T
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000589949
  gene symbol: H3F3B
  hgvsc: ENST00000589949.1:n.316C>T
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000468714
  ensembl transcript: ENST00000587560
  gene symbol: H3F3B
  hgvsc: ENST00000587560.1:c.129-16C>T
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000254810
  ensembl transcript: ENST00000254810
  gene symbol: H3F3B
  hgvsc: ENST00000254810.4:c.129-16C>T
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000465813
  ensembl transcript: ENST00000589599
  gene symbol: H3F3B
  hgvsc: ENST00000589599.1:c.129-16C>T
  variant of: http://identifiers.org/hgnc/4765
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 681
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 30686
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11634
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1502
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 632
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2149
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12281
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 595
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Latino
population: African
population: Other
reference allele: G
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: DP

17-73775063-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73775063
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 73775063
    reference: chr 17
allele count: 3
allele frequency: 2.506307540643954e-5
allele num: 119698
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000589417
  gene symbol: H3F3B
  hgvsc: ENST00000589417.1:n.326C>T
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000593254
  gene symbol: H3F3B
  hgvsc: ENST00000593254.1:n.118-100C>T
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000466663
  ensembl transcript: ENST00000591890
  gene symbol: H3F3B
  hgvsc: ENST00000591890.1:c.129-19C>T
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000465813
  ensembl transcript: ENST00000589599
  gene symbol: H3F3B
  hgvsc: ENST00000589599.1:c.129-19C>T
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000589949
  gene symbol: H3F3B
  hgvsc: ENST00000589949.1:n.313C>T
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000466020
  ensembl transcript: ENST00000586607
  gene symbol: H3F3B
  hgvsc: ENST00000586607.1:c.129-19C>T
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000467165
  ensembl transcript: ENST00000592643
  gene symbol: H3F3B
  hgvsc: ENST00000592643.1:c.129-19C>T
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000465403
  ensembl transcript: ENST00000586270
  gene symbol: H3F3B
  hgvsc: ENST00000586270.1:c.129-19C>T
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000586518
  gene symbol: H3F3B
  hgvsc: ENST00000586518.1:n.791C>T
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000468484
  ensembl transcript: ENST00000587171
  gene symbol: H3F3B
  hgvsc: ENST00000587171.1:c.129-19C>T
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000468714
  ensembl transcript: ENST00000587560
  gene symbol: H3F3B
  hgvsc: ENST00000587560.1:c.129-19C>T
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000254810
  ensembl transcript: ENST00000254810
  gene symbol: H3F3B
  hgvsc: ENST00000254810.4:c.129-19C>T
  variant of: http://identifiers.org/hgnc/4765
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 983
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 586
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1867
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30303
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11526
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2115
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 685
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12082
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: African
population: Latino
population: East Asian
population: South Asian
reference allele: G
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff

17-73775065-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73775065
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 73775065
    reference: chr 17
allele count: 1
allele frequency: 8.368480953337351e-6
allele num: 119496
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000586518
  gene symbol: H3F3B
  hgvsc: ENST00000586518.1:n.789C>T
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000593254
  gene symbol: H3F3B
  hgvsc: ENST00000593254.1:n.118-102C>T
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000466020
  ensembl transcript: ENST00000586607
  gene symbol: H3F3B
  hgvsc: ENST00000586607.1:c.129-21C>T
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000468714
  ensembl transcript: ENST00000587560
  gene symbol: H3F3B
  hgvsc: ENST00000587560.1:c.129-21C>T
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000466663
  ensembl transcript: ENST00000591890
  gene symbol: H3F3B
  hgvsc: ENST00000591890.1:c.129-21C>T
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000465403
  ensembl transcript: ENST00000586270
  gene symbol: H3F3B
  hgvsc: ENST00000586270.1:c.129-21C>T
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000589417
  gene symbol: H3F3B
  hgvsc: ENST00000589417.1:n.324C>T
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000468484
  ensembl transcript: ENST00000587171
  gene symbol: H3F3B
  hgvsc: ENST00000587171.1:c.129-21C>T
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000467165
  ensembl transcript: ENST00000592643
  gene symbol: H3F3B
  hgvsc: ENST00000592643.1:c.129-21C>T
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000589949
  gene symbol: H3F3B
  hgvsc: ENST00000589949.1:n.311C>T
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000254810
  ensembl transcript: ENST00000254810
  gene symbol: H3F3B
  hgvsc: ENST00000254810.4:c.129-21C>T
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000465813
  ensembl transcript: ENST00000589599
  gene symbol: H3F3B
  hgvsc: ENST00000589599.1:c.129-21C>T
  variant of: http://identifiers.org/hgnc/4765
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11527
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2163
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11847
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2067
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1297
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 580
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29892
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 749
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: East Asian
population: Other
reference allele: G
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: MQ

17-73775066-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73775066
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 73775066
    reference: chr 17
allele count: 1
allele frequency: 8.370021929457456e-6
allele num: 119474
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000466020
  ensembl transcript: ENST00000586607
  gene symbol: H3F3B
  hgvsc: ENST00000586607.1:c.129-22A>G
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000254810
  ensembl transcript: ENST00000254810
  gene symbol: H3F3B
  hgvsc: ENST00000254810.4:c.129-22A>G
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000465403
  ensembl transcript: ENST00000586270
  gene symbol: H3F3B
  hgvsc: ENST00000586270.1:c.129-22A>G
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000586518
  gene symbol: H3F3B
  hgvsc: ENST00000586518.1:n.788A>G
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000589949
  gene symbol: H3F3B
  hgvsc: ENST00000589949.1:n.310A>G
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000468484
  ensembl transcript: ENST00000587171
  gene symbol: H3F3B
  hgvsc: ENST00000587171.1:c.129-22A>G
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000468714
  ensembl transcript: ENST00000587560
  gene symbol: H3F3B
  hgvsc: ENST00000587560.1:c.129-22A>G
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000589417
  gene symbol: H3F3B
  hgvsc: ENST00000589417.1:n.323A>G
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000465813
  ensembl transcript: ENST00000589599
  gene symbol: H3F3B
  hgvsc: ENST00000589599.1:c.129-22A>G
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000466663
  ensembl transcript: ENST00000591890
  gene symbol: H3F3B
  hgvsc: ENST00000591890.1:c.129-22A>G
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000467165
  ensembl transcript: ENST00000592643
  gene symbol: H3F3B
  hgvsc: ENST00000592643.1:c.129-22A>G
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000593254
  gene symbol: H3F3B
  hgvsc: ENST00000593254.1:n.118-103A>G
  variant of: http://identifiers.org/hgnc/4765
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 580
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11537
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11818
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1298
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2164
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2062
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 754
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29911
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: African
population: South Asian
population: East Asian
population: Other
population: European (Finnish)
reference allele: T
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ

17-73775069-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73775069
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 73775069
    reference: chr 17
allele count: 1
allele frequency: 8.389684044498884e-6
allele num: 119194
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000465403
  ensembl transcript: ENST00000586270
  gene symbol: H3F3B
  hgvsc: ENST00000586270.1:c.129-25C>T
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000466663
  ensembl transcript: ENST00000591890
  gene symbol: H3F3B
  hgvsc: ENST00000591890.1:c.129-25C>T
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000254810
  ensembl transcript: ENST00000254810
  gene symbol: H3F3B
  hgvsc: ENST00000254810.4:c.129-25C>T
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000589949
  gene symbol: H3F3B
  hgvsc: ENST00000589949.1:n.307C>T
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000593254
  gene symbol: H3F3B
  hgvsc: ENST00000593254.1:n.118-106C>T
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000589417
  gene symbol: H3F3B
  hgvsc: ENST00000589417.1:n.320C>T
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000468714
  ensembl transcript: ENST00000587560
  gene symbol: H3F3B
  hgvsc: ENST00000587560.1:c.129-25C>T
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000465813
  ensembl transcript: ENST00000589599
  gene symbol: H3F3B
  hgvsc: ENST00000589599.1:c.129-25C>T
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000586518
  gene symbol: H3F3B
  hgvsc: ENST00000586518.1:n.785C>T
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000466020
  ensembl transcript: ENST00000586607
  gene symbol: H3F3B
  hgvsc: ENST00000586607.1:c.129-25C>T
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000467165
  ensembl transcript: ENST00000592643
  gene symbol: H3F3B
  hgvsc: ENST00000592643.1:c.129-25C>T
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000468484
  ensembl transcript: ENST00000587171
  gene symbol: H3F3B
  hgvsc: ENST00000587171.1:c.129-25C>T
  variant of: http://identifiers.org/hgnc/4765
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29506
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1967
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11676
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1647
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11376
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2501
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 860
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 570
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: East Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: Latino
population: South Asian
reference allele: G
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum

17-73775071-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73775071
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 73775071
    reference: chr 17
allele count: 4
allele frequency: 3.359368438733518e-5
allele num: 119070
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000593254
  gene symbol: H3F3B
  hgvsc: ENST00000593254.1:n.118-108C>T
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000254810
  ensembl transcript: ENST00000254810
  gene symbol: H3F3B
  hgvsc: ENST00000254810.4:c.129-27C>T
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000466663
  ensembl transcript: ENST00000591890
  gene symbol: H3F3B
  hgvsc: ENST00000591890.1:c.129-27C>T
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000466020
  ensembl transcript: ENST00000586607
  gene symbol: H3F3B
  hgvsc: ENST00000586607.1:c.129-27C>T
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000468484
  ensembl transcript: ENST00000587171
  gene symbol: H3F3B
  hgvsc: ENST00000587171.1:c.129-27C>T
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000465813
  ensembl transcript: ENST00000589599
  gene symbol: H3F3B
  hgvsc: ENST00000589599.1:c.129-27C>T
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000589949
  gene symbol: H3F3B
  hgvsc: ENST00000589949.1:n.305C>T
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000467165
  ensembl transcript: ENST00000592643
  gene symbol: H3F3B
  hgvsc: ENST00000592643.1:c.129-27C>T
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000468714
  ensembl transcript: ENST00000587560
  gene symbol: H3F3B
  hgvsc: ENST00000587560.1:c.129-27C>T
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000589417
  gene symbol: H3F3B
  hgvsc: ENST00000589417.1:n.318C>T
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000465403
  ensembl transcript: ENST00000586270
  gene symbol: H3F3B
  hgvsc: ENST00000586270.1:c.129-27C>T
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000586518
  gene symbol: H3F3B
  hgvsc: ENST00000586518.1:n.783C>T
  variant of: http://identifiers.org/hgnc/4765
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 29457
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11861
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 896
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1879
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1753
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2600
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: Other
population: East Asian
population: South Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: MQ

17-73775071-GGACGCT-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73775071
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 73775065
    reference: chr 17
allele count: 1
allele frequency: 8.398421096833796e-6
allele num: 119070
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000254810
  ensembl transcript: ENST00000254810
  gene symbol: H3F3B
  hgvsc: ENST00000254810.4:c.129-33_129-28delAGCGTC
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000589417
  gene symbol: H3F3B
  hgvsc: ENST00000589417.1:n.312_317delAGCGTC
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000467165
  ensembl transcript: ENST00000592643
  gene symbol: H3F3B
  hgvsc: ENST00000592643.1:c.129-33_129-28delAGCGTC
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000589949
  gene symbol: H3F3B
  hgvsc: ENST00000589949.1:n.299_304delAGCGTC
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000465813
  ensembl transcript: ENST00000589599
  gene symbol: H3F3B
  hgvsc: ENST00000589599.1:c.129-33_129-28delAGCGTC
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000593254
  gene symbol: H3F3B
  hgvsc: ENST00000593254.1:n.118-114_118-109delAGCGTC
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000586518
  gene symbol: H3F3B
  hgvsc: ENST00000586518.1:n.777_782delAGCGTC
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000468484
  ensembl transcript: ENST00000587171
  gene symbol: H3F3B
  hgvsc: ENST00000587171.1:c.129-33_129-28delAGCGTC
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000466663
  ensembl transcript: ENST00000591890
  gene symbol: H3F3B
  hgvsc: ENST00000591890.1:c.129-33_129-28delAGCGTC
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000466020
  ensembl transcript: ENST00000586607
  gene symbol: H3F3B
  hgvsc: ENST00000586607.1:c.129-33_129-28delAGCGTC
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000465403
  ensembl transcript: ENST00000586270
  gene symbol: H3F3B
  hgvsc: ENST00000586270.1:c.129-33_129-28delAGCGTC
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000468714
  ensembl transcript: ENST00000587560
  gene symbol: H3F3B
  hgvsc: ENST00000587560.1:c.129-33_129-28delAGCGTC
  variant of: http://identifiers.org/hgnc/4765
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1753
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11108
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11861
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1879
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 896
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2600
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29457
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: African
population: Other
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Latino
reference allele: GGACGCT
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS

17-73775072-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73775072
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 73775072
    reference: chr 17
allele count: 10
allele frequency: 8.398562166157153e-5
allele num: 119068
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000589417
  gene symbol: H3F3B
  hgvsc: ENST00000589417.1:n.317C>T
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000465813
  ensembl transcript: ENST00000589599
  gene symbol: H3F3B
  hgvsc: ENST00000589599.1:c.129-28C>T
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000466020
  ensembl transcript: ENST00000586607
  gene symbol: H3F3B
  hgvsc: ENST00000586607.1:c.129-28C>T
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000466663
  ensembl transcript: ENST00000591890
  gene symbol: H3F3B
  hgvsc: ENST00000591890.1:c.129-28C>T
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000468484
  ensembl transcript: ENST00000587171
  gene symbol: H3F3B
  hgvsc: ENST00000587171.1:c.129-28C>T
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000465403
  ensembl transcript: ENST00000586270
  gene symbol: H3F3B
  hgvsc: ENST00000586270.1:c.129-28C>T
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000593254
  gene symbol: H3F3B
  hgvsc: ENST00000593254.1:n.118-109C>T
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000254810
  ensembl transcript: ENST00000254810
  gene symbol: H3F3B
  hgvsc: ENST00000254810.4:c.129-28C>T
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000586518
  gene symbol: H3F3B
  hgvsc: ENST00000586518.1:n.782C>T
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000467165
  ensembl transcript: ENST00000592643
  gene symbol: H3F3B
  hgvsc: ENST00000592643.1:c.129-28C>T
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000589949
  gene symbol: H3F3B
  hgvsc: ENST00000589949.1:n.304C>T
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000468714
  ensembl transcript: ENST00000587560
  gene symbol: H3F3B
  hgvsc: ENST00000587560.1:c.129-28C>T
  variant of: http://identifiers.org/hgnc/4765
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1741
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11057
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 904
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 5.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 29480
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 538
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2600
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1862
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11917
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: African
population: Other
population: Latino
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum

17-73775074-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73775074
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 73775074
    reference: chr 17
allele count: 8
allele frequency: 6.726645926175061e-5
allele num: 118930
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000465403
  ensembl transcript: ENST00000586270
  gene symbol: H3F3B
  hgvsc: ENST00000586270.1:c.129-30G>A
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000466663
  ensembl transcript: ENST00000591890
  gene symbol: H3F3B
  hgvsc: ENST00000591890.1:c.129-30G>A
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000593254
  gene symbol: H3F3B
  hgvsc: ENST00000593254.1:n.118-111G>A
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000467165
  ensembl transcript: ENST00000592643
  gene symbol: H3F3B
  hgvsc: ENST00000592643.1:c.129-30G>A
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000589417
  gene symbol: H3F3B
  hgvsc: ENST00000589417.1:n.315G>A
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000586518
  gene symbol: H3F3B
  hgvsc: ENST00000586518.1:n.780G>A
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000468714
  ensembl transcript: ENST00000587560
  gene symbol: H3F3B
  hgvsc: ENST00000587560.1:c.129-30G>A
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000589949
  gene symbol: H3F3B
  hgvsc: ENST00000589949.1:n.302G>A
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000466020
  ensembl transcript: ENST00000586607
  gene symbol: H3F3B
  hgvsc: ENST00000586607.1:c.129-30G>A
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000465813
  ensembl transcript: ENST00000589599
  gene symbol: H3F3B
  hgvsc: ENST00000589599.1:c.129-30G>A
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000468484
  ensembl transcript: ENST00000587171
  gene symbol: H3F3B
  hgvsc: ENST00000587171.1:c.129-30G>A
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000254810
  ensembl transcript: ENST00000254810
  gene symbol: H3F3B
  hgvsc: ENST00000254810.4:c.129-30G>A
  variant of: http://identifiers.org/hgnc/4765
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10824
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 946
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2736
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1871
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1798
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12060
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29331
  bin: 2.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: Other
population: South Asian
reference allele: C
site quality: QD
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum

17-73775078-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73775078
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 73775078
    reference: chr 17
allele count: 2
allele frequency: 1.691160305085319e-5
allele num: 118262
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000589417
  gene symbol: H3F3B
  hgvsc: ENST00000589417.1:n.311C>T
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000467165
  ensembl transcript: ENST00000592643
  gene symbol: H3F3B
  hgvsc: ENST00000592643.1:c.129-34C>T
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000589949
  gene symbol: H3F3B
  hgvsc: ENST00000589949.1:n.298C>T
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000468484
  ensembl transcript: ENST00000587171
  gene symbol: H3F3B
  hgvsc: ENST00000587171.1:c.129-34C>T
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000254810
  ensembl transcript: ENST00000254810
  gene symbol: H3F3B
  hgvsc: ENST00000254810.4:c.129-34C>T
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000466020
  ensembl transcript: ENST00000586607
  gene symbol: H3F3B
  hgvsc: ENST00000586607.1:c.129-34C>T
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000466663
  ensembl transcript: ENST00000591890
  gene symbol: H3F3B
  hgvsc: ENST00000591890.1:c.129-34C>T
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000586518
  gene symbol: H3F3B
  hgvsc: ENST00000586518.1:n.776C>T
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000465813
  ensembl transcript: ENST00000589599
  gene symbol: H3F3B
  hgvsc: ENST00000589599.1:c.129-34C>T
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000468714
  ensembl transcript: ENST00000587560
  gene symbol: H3F3B
  hgvsc: ENST00000587560.1:c.129-34C>T
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000465403
  ensembl transcript: ENST00000586270
  gene symbol: H3F3B
  hgvsc: ENST00000586270.1:c.129-34C>T
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000593254
  gene symbol: H3F3B
  hgvsc: ENST00000593254.1:n.118-115C>T
  variant of: http://identifiers.org/hgnc/4765
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12181
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1109
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3355
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28272
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2785
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1694
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 509
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10144
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: East Asian
population: European (Finnish)
population: South Asian
population: Other
population: Latino
reference allele: G
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: QD

http://identifiers.org/exac.variant/17-73775085-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73775085
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 73775085
    reference: chr 17
allele count: 1
allele frequency: 8.465536799688468e-6
allele num: 118126
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000465813
  ensembl transcript: ENST00000589599
  gene symbol: H3F3B
  hgvsc: ENST00000589599.1:c.129-41T>G
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000586518
  gene symbol: H3F3B
  hgvsc: ENST00000586518.1:n.769T>G
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000254810
  ensembl transcript: ENST00000254810
  gene symbol: H3F3B
  hgvsc: ENST00000254810.4:c.129-41T>G
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000589417
  gene symbol: H3F3B
  hgvsc: ENST00000589417.1:n.304T>G
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000468484
  ensembl transcript: ENST00000587171
  gene symbol: H3F3B
  hgvsc: ENST00000587171.1:c.129-41T>G
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000467165
  ensembl transcript: ENST00000592643
  gene symbol: H3F3B
  hgvsc: ENST00000592643.1:c.129-41T>G
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000466663
  ensembl transcript: ENST00000591890
  gene symbol: H3F3B
  hgvsc: ENST00000591890.1:c.129-41T>G
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000466020
  ensembl transcript: ENST00000586607
  gene symbol: H3F3B
  hgvsc: ENST00000586607.1:c.129-41T>G
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000589949
  gene symbol: H3F3B
  hgvsc: ENST00000589949.1:n.291T>G
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000465403
  ensembl transcript: ENST00000586270
  gene symbol: H3F3B
  hgvsc: ENST00000586270.1:c.129-41T>G
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000468714
  ensembl transcript: ENST00000587560
  gene symbol: H3F3B
  hgvsc: ENST00000587560.1:c.129-41T>G
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000593254
  gene symbol: H3F3B
  hgvsc: ENST00000593254.1:n.118-122T>G
  variant of: http://identifiers.org/hgnc/4765
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12630
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9430
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3278
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27657
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 463
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1252
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3725
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1592
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: Latino
population: African
population: South Asian
population: European (Finnish)
population: East Asian
reference allele: A
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/17-73775089-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73775089
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 73775089
    reference: chr 17
allele count: 1
allele frequency: 8.528493697443158e-6
allele num: 117254
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000466020
  ensembl transcript: ENST00000586607
  gene symbol: H3F3B
  hgvsc: ENST00000586607.1:c.128+39G>T
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000465403
  ensembl transcript: ENST00000586270
  gene symbol: H3F3B
  hgvsc: ENST00000586270.1:c.128+39G>T
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000467165
  ensembl transcript: ENST00000592643
  gene symbol: H3F3B
  hgvsc: ENST00000592643.1:c.128+39G>T
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000589949
  gene symbol: H3F3B
  hgvsc: ENST00000589949.1:n.287G>T
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000589417
  gene symbol: H3F3B
  hgvsc: ENST00000589417.1:n.300G>T
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000254810
  ensembl transcript: ENST00000254810
  gene symbol: H3F3B
  hgvsc: ENST00000254810.4:c.128+39G>T
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000466663
  ensembl transcript: ENST00000591890
  gene symbol: H3F3B
  hgvsc: ENST00000591890.1:c.128+39G>T
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000465813
  ensembl transcript: ENST00000589599
  gene symbol: H3F3B
  hgvsc: ENST00000589599.1:c.128+39G>T
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000468714
  ensembl transcript: ENST00000587560
  gene symbol: H3F3B
  hgvsc: ENST00000587560.1:c.128+39G>T
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000586518
  gene symbol: H3F3B
  hgvsc: ENST00000586518.1:n.765G>T
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000593254
  gene symbol: H3F3B
  hgvsc: ENST00000593254.1:n.118-126G>T
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000468484
  ensembl transcript: ENST00000587171
  gene symbol: H3F3B
  hgvsc: ENST00000587171.1:c.128+39G>T
  variant of: http://identifiers.org/hgnc/4765
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4232
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1331
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 434
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 26164
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4457
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1477
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13701
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8185
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: Other
population: Latino
population: European (Non-Finnish)
population: African
population: East Asian
population: European (Finnish)
reference allele: C
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP

17-73775093-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73775093
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 73775093
    reference: chr 17
allele count: 16
allele frequency: 1.363303283856785e-4
allele num: 117362
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000468484
  ensembl transcript: ENST00000587171
  gene symbol: H3F3B
  hgvsc: ENST00000587171.1:c.128+35G>A
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000467165
  ensembl transcript: ENST00000592643
  gene symbol: H3F3B
  hgvsc: ENST00000592643.1:c.128+35G>A
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000465813
  ensembl transcript: ENST00000589599
  gene symbol: H3F3B
  hgvsc: ENST00000589599.1:c.128+35G>A
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000468714
  ensembl transcript: ENST00000587560
  gene symbol: H3F3B
  hgvsc: ENST00000587560.1:c.128+35G>A
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000466663
  ensembl transcript: ENST00000591890
  gene symbol: H3F3B
  hgvsc: ENST00000591890.1:c.128+35G>A
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000254810
  ensembl transcript: ENST00000254810
  gene symbol: H3F3B
  hgvsc: ENST00000254810.4:c.128+35G>A
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000586518
  gene symbol: H3F3B
  hgvsc: ENST00000586518.1:n.761G>A
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000593254
  gene symbol: H3F3B
  hgvsc: ENST00000593254.1:n.118-130G>A
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000589949
  gene symbol: H3F3B
  hgvsc: ENST00000589949.1:n.283G>A
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000589417
  gene symbol: H3F3B
  hgvsc: ENST00000589417.1:n.296G>A
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000465403
  ensembl transcript: ENST00000586270
  gene symbol: H3F3B
  hgvsc: ENST00000586270.1:c.128+35G>A
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000466020
  ensembl transcript: ENST00000586607
  gene symbol: H3F3B
  hgvsc: ENST00000586607.1:c.128+35G>A
  variant of: http://identifiers.org/hgnc/4765
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4355
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4245
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1523
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1257
  bin: 3.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14436
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 7631
  bin: 3.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 419
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26118
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: Other
population: European (Finnish)
population: South Asian
population: Latino
population: European (Non-Finnish)
population: African
reference allele: C
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: ClippingRankSum

17-73775095-A-ACCG
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73775095
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 73775098
    reference: chr 17
allele count: 1
allele frequency: 8.532568815167494e-6
allele num: 117198
alternate allele: ACCG
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000465403
  ensembl transcript: ENST00000586270
  gene symbol: H3F3B
  hgvsc: ENST00000586270.1:c.128+30_128+32dupCGG
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000465813
  ensembl transcript: ENST00000589599
  gene symbol: H3F3B
  hgvsc: ENST00000589599.1:c.128+30_128+32dupCGG
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000586518
  gene symbol: H3F3B
  hgvsc: ENST00000586518.1:n.756_758dupCGG
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000467165
  ensembl transcript: ENST00000592643
  gene symbol: H3F3B
  hgvsc: ENST00000592643.1:c.128+30_128+32dupCGG
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000254810
  ensembl transcript: ENST00000254810
  gene symbol: H3F3B
  hgvsc: ENST00000254810.4:c.128+30_128+32dupCGG
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000589949
  gene symbol: H3F3B
  hgvsc: ENST00000589949.1:n.278_280dupCGG
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000589417
  gene symbol: H3F3B
  hgvsc: ENST00000589417.1:n.291_293dupCGG
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000466663
  ensembl transcript: ENST00000591890
  gene symbol: H3F3B
  hgvsc: ENST00000591890.1:c.128+30_128+32dupCGG
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000468484
  ensembl transcript: ENST00000587171
  gene symbol: H3F3B
  hgvsc: ENST00000587171.1:c.128+30_128+32dupCGG
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000468714
  ensembl transcript: ENST00000587560
  gene symbol: H3F3B
  hgvsc: ENST00000587560.1:c.128+30_128+32dupCGG
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000593254
  gene symbol: H3F3B
  hgvsc: ENST00000593254.1:n.118-135_118-133dupCGG
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000466020
  ensembl transcript: ENST00000586607
  gene symbol: H3F3B
  hgvsc: ENST00000586607.1:c.128+30_128+32dupCGG
  variant of: http://identifiers.org/hgnc/4765
canonical: false
consequence: non coding transcript exon
filter: VQSRTrancheINDEL97.00to99.00
genotype depth: GenotypeDepth
  all individuals: 7387
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1213
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4332
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1559
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 412
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4517
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25751
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14811
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Other
population: European (Non-Finnish)
population: African
population: East Asian
population: Latino
reference allele: A
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: MQ

17-73775097-CGCCGGGCCATT-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73775097
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 73775086
    reference: chr 17
allele count: 2
allele frequency: 1.705989729941826e-5
allele num: 117234
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000593254
  gene symbol: H3F3B
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000466020
  ensembl transcript: ENST00000586607
  gene symbol: H3F3B
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000468484
  ensembl transcript: ENST00000587171
  gene symbol: H3F3B
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000586518
  gene symbol: H3F3B
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000254810
  ensembl transcript: ENST00000254810
  gene symbol: H3F3B
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000468714
  ensembl transcript: ENST00000587560
  gene symbol: H3F3B
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000589417
  gene symbol: H3F3B
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000467165
  ensembl transcript: ENST00000592643
  gene symbol: H3F3B
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000466663
  ensembl transcript: ENST00000591890
  gene symbol: H3F3B
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000465403
  ensembl transcript: ENST00000586270
  gene symbol: H3F3B
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000589949
  gene symbol: H3F3B
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000465813
  ensembl transcript: ENST00000589599
  gene symbol: H3F3B
  variant of: http://identifiers.org/hgnc/4765
canonical: false
consequence: non coding transcript exon
filter: VQSRTrancheINDEL97.00to99.00
genotype depth: GenotypeDepth
  all individuals: 320
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7274
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1593
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25512
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15002
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4402
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4579
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1205
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 411
  bin: 4.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1968
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 413
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Other
reference allele: CGCCGGGCCATT
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ

17-73775100-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73775100
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 73775100
    reference: chr 17
allele count: 3
allele frequency: 2.562306759365231e-5
allele num: 117082
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000465813
  ensembl transcript: ENST00000589599
  gene symbol: H3F3B
  hgvsc: ENST00000589599.1:c.128+28G>C
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000254810
  ensembl transcript: ENST00000254810
  gene symbol: H3F3B
  hgvsc: ENST00000254810.4:c.128+28G>C
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000589417
  gene symbol: H3F3B
  hgvsc: ENST00000589417.1:n.289G>C
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000466020
  ensembl transcript: ENST00000586607
  gene symbol: H3F3B
  hgvsc: ENST00000586607.1:c.128+28G>C
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000589949
  gene symbol: H3F3B
  hgvsc: ENST00000589949.1:n.276G>C
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000586518
  gene symbol: H3F3B
  hgvsc: ENST00000586518.1:n.754G>C
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000466663
  ensembl transcript: ENST00000591890
  gene symbol: H3F3B
  hgvsc: ENST00000591890.1:c.128+28G>C
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000468484
  ensembl transcript: ENST00000587171
  gene symbol: H3F3B
  hgvsc: ENST00000587171.1:c.128+28G>C
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000467165
  ensembl transcript: ENST00000592643
  gene symbol: H3F3B
  hgvsc: ENST00000592643.1:c.128+28G>C
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000468714
  ensembl transcript: ENST00000587560
  gene symbol: H3F3B
  hgvsc: ENST00000587560.1:c.128+28G>C
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000465403
  ensembl transcript: ENST00000586270
  gene symbol: H3F3B
  hgvsc: ENST00000586270.1:c.128+28G>C
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000593254
  gene symbol: H3F3B
  hgvsc: ENST00000593254.1:n.118-137G>C
  variant of: http://identifiers.org/hgnc/4765
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 25056
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15442
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4523
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4746
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1167
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1658
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 327
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6991
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Latino
population: South Asian
population: African
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: MQRankSum

17-73775101-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73775101
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 73775101
    reference: chr 17
allele count: 12
allele frequency: 1.024712653493416e-4
allele num: 117106
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000593254
  gene symbol: H3F3B
  hgvsc: ENST00000593254.1:n.118-138C>T
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000589949
  gene symbol: H3F3B
  hgvsc: ENST00000589949.1:n.275C>T
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000586518
  gene symbol: H3F3B
  hgvsc: ENST00000586518.1:n.753C>T
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000467165
  ensembl transcript: ENST00000592643
  gene symbol: H3F3B
  hgvsc: ENST00000592643.1:c.128+27C>T
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000465813
  ensembl transcript: ENST00000589599
  gene symbol: H3F3B
  hgvsc: ENST00000589599.1:c.128+27C>T
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000466020
  ensembl transcript: ENST00000586607
  gene symbol: H3F3B
  hgvsc: ENST00000586607.1:c.128+27C>T
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000465403
  ensembl transcript: ENST00000586270
  gene symbol: H3F3B
  hgvsc: ENST00000586270.1:c.128+27C>T
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000468484
  ensembl transcript: ENST00000587171
  gene symbol: H3F3B
  hgvsc: ENST00000587171.1:c.128+27C>T
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000589417
  gene symbol: H3F3B
  hgvsc: ENST00000589417.1:n.288C>T
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000466663
  ensembl transcript: ENST00000591890
  gene symbol: H3F3B
  hgvsc: ENST00000591890.1:c.128+27C>T
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000254810
  ensembl transcript: ENST00000254810
  gene symbol: H3F3B
  hgvsc: ENST00000254810.4:c.128+27C>T
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000468714
  ensembl transcript: ENST00000587560
  gene symbol: H3F3B
  hgvsc: ENST00000587560.1:c.128+27C>T
  variant of: http://identifiers.org/hgnc/4765
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15674
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6915
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4687
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4549
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1676
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1165
  bin: 3.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 4.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Other
population: Latino
population: South Asian
population: East Asian
reference allele: G
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum

17-73775102-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73775102
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 73775102
    reference: chr 17
allele count: 1
allele frequency: 8.534025158306167e-6
allele num: 117178
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000589949
  gene symbol: H3F3B
  hgvsc: ENST00000589949.1:n.274C>T
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000254810
  ensembl transcript: ENST00000254810
  gene symbol: H3F3B
  hgvsc: ENST00000254810.4:c.128+26C>T
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000465813
  ensembl transcript: ENST00000589599
  gene symbol: H3F3B
  hgvsc: ENST00000589599.1:c.128+26C>T
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000466663
  ensembl transcript: ENST00000591890
  gene symbol: H3F3B
  hgvsc: ENST00000591890.1:c.128+26C>T
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000468714
  ensembl transcript: ENST00000587560
  gene symbol: H3F3B
  hgvsc: ENST00000587560.1:c.128+26C>T
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000466020
  ensembl transcript: ENST00000586607
  gene symbol: H3F3B
  hgvsc: ENST00000586607.1:c.128+26C>T
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000468484
  ensembl transcript: ENST00000587171
  gene symbol: H3F3B
  hgvsc: ENST00000587171.1:c.128+26C>T
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000589417
  gene symbol: H3F3B
  hgvsc: ENST00000589417.1:n.287C>T
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000586518
  gene symbol: H3F3B
  hgvsc: ENST00000586518.1:n.752C>T
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000465403
  ensembl transcript: ENST00000586270
  gene symbol: H3F3B
  hgvsc: ENST00000586270.1:c.128+26C>T
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000593254
  gene symbol: H3F3B
  hgvsc: ENST00000593254.1:n.118-139C>T
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000467165
  ensembl transcript: ENST00000592643
  gene symbol: H3F3B
  hgvsc: ENST00000592643.1:c.128+26C>T
  variant of: http://identifiers.org/hgnc/4765
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1145
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4601
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15771
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1685
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4790
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24786
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6823
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: East Asian
population: African
population: South Asian
reference allele: G
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: DP

17-73775102-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73775102
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 73775102
    reference: chr 17
allele count: 2
allele frequency: 1.706805031661233e-5
allele num: 117178
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000468714
  ensembl transcript: ENST00000587560
  gene symbol: H3F3B
  hgvsc: ENST00000587560.1:c.128+26C>G
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000467165
  ensembl transcript: ENST00000592643
  gene symbol: H3F3B
  hgvsc: ENST00000592643.1:c.128+26C>G
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000589417
  gene symbol: H3F3B
  hgvsc: ENST00000589417.1:n.287C>G
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000589949
  gene symbol: H3F3B
  hgvsc: ENST00000589949.1:n.274C>G
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000466020
  ensembl transcript: ENST00000586607
  gene symbol: H3F3B
  hgvsc: ENST00000586607.1:c.128+26C>G
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000586518
  gene symbol: H3F3B
  hgvsc: ENST00000586518.1:n.752C>G
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000593254
  gene symbol: H3F3B
  hgvsc: ENST00000593254.1:n.118-139C>G
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000466663
  ensembl transcript: ENST00000591890
  gene symbol: H3F3B
  hgvsc: ENST00000591890.1:c.128+26C>G
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000254810
  ensembl transcript: ENST00000254810
  gene symbol: H3F3B
  hgvsc: ENST00000254810.4:c.128+26C>G
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000465813
  ensembl transcript: ENST00000589599
  gene symbol: H3F3B
  hgvsc: ENST00000589599.1:c.128+26C>G
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000465403
  ensembl transcript: ENST00000586270
  gene symbol: H3F3B
  hgvsc: ENST00000586270.1:c.128+26C>G
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000468484
  ensembl transcript: ENST00000587171
  gene symbol: H3F3B
  hgvsc: ENST00000587171.1:c.128+26C>G
  variant of: http://identifiers.org/hgnc/4765
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4601
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4790
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24786
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1685
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6823
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15771
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1145
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: South Asian
population: East Asian
population: Latino
population: European (Non-Finnish)
population: Other
population: European (Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP

17-73775103-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73775103
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 73775103
    reference: chr 17
allele count: 1
allele frequency: 8.539563799081142e-6
allele num: 117102
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000589949
  gene symbol: H3F3B
  hgvsc: ENST00000589949.1:n.273C>T
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000465813
  ensembl transcript: ENST00000589599
  gene symbol: H3F3B
  hgvsc: ENST00000589599.1:c.128+25C>T
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000465403
  ensembl transcript: ENST00000586270
  gene symbol: H3F3B
  hgvsc: ENST00000586270.1:c.128+25C>T
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000254810
  ensembl transcript: ENST00000254810
  gene symbol: H3F3B
  hgvsc: ENST00000254810.4:c.128+25C>T
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000589417
  gene symbol: H3F3B
  hgvsc: ENST00000589417.1:n.286C>T
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000586518
  gene symbol: H3F3B
  hgvsc: ENST00000586518.1:n.751C>T
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000466663
  ensembl transcript: ENST00000591890
  gene symbol: H3F3B
  hgvsc: ENST00000591890.1:c.128+25C>T
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000466020
  ensembl transcript: ENST00000586607
  gene symbol: H3F3B
  hgvsc: ENST00000586607.1:c.128+25C>T
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000467165
  ensembl transcript: ENST00000592643
  gene symbol: H3F3B
  hgvsc: ENST00000592643.1:c.128+25C>T
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000593254
  gene symbol: H3F3B
  hgvsc: ENST00000593254.1:n.118-140C>T
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000468714
  ensembl transcript: ENST00000587560
  gene symbol: H3F3B
  hgvsc: ENST00000587560.1:c.128+25C>T
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000468484
  ensembl transcript: ENST00000587171
  gene symbol: H3F3B
  hgvsc: ENST00000587171.1:c.128+25C>T
  variant of: http://identifiers.org/hgnc/4765
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24666
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1138
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15767
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1694
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4914
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6783
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4641
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: African
population: European (Non-Finnish)
population: East Asian
population: Latino
population: European (Finnish)
population: Other
reference allele: G
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum

17-73775106-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73775106
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 73775106
    reference: chr 17
allele count: 1
allele frequency: 8.542043940274029e-6
allele num: 117068
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000254810
  ensembl transcript: ENST00000254810
  gene symbol: H3F3B
  hgvsc: ENST00000254810.4:c.128+22T>C
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000589949
  gene symbol: H3F3B
  hgvsc: ENST00000589949.1:n.270T>C
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000465813
  ensembl transcript: ENST00000589599
  gene symbol: H3F3B
  hgvsc: ENST00000589599.1:c.128+22T>C
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000468484
  ensembl transcript: ENST00000587171
  gene symbol: H3F3B
  hgvsc: ENST00000587171.1:c.128+22T>C
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000466020
  ensembl transcript: ENST00000586607
  gene symbol: H3F3B
  hgvsc: ENST00000586607.1:c.128+22T>C
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000466663
  ensembl transcript: ENST00000591890
  gene symbol: H3F3B
  hgvsc: ENST00000591890.1:c.128+22T>C
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000589417
  gene symbol: H3F3B
  hgvsc: ENST00000589417.1:n.283T>C
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000593254
  gene symbol: H3F3B
  hgvsc: ENST00000593254.1:n.118-143T>C
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000586518
  gene symbol: H3F3B
  hgvsc: ENST00000586518.1:n.748T>C
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000467165
  ensembl transcript: ENST00000592643
  gene symbol: H3F3B
  hgvsc: ENST00000592643.1:c.128+22T>C
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000465403
  ensembl transcript: ENST00000586270
  gene symbol: H3F3B
  hgvsc: ENST00000586270.1:c.128+22T>C
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000468714
  ensembl transcript: ENST00000587560
  gene symbol: H3F3B
  hgvsc: ENST00000587560.1:c.128+22T>C
  variant of: http://identifiers.org/hgnc/4765
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6596
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 327
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16059
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4770
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1734
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1116
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24234
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: Latino
population: South Asian
population: African
population: East Asian
population: European (Finnish)
reference allele: A
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum

17-73775107-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73775107
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 73775107
    reference: chr 17
allele count: 2
allele frequency: 1.70919719007982e-5
allele num: 117014
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000589949
  gene symbol: H3F3B
  hgvsc: ENST00000589949.1:n.269A>G
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000589417
  gene symbol: H3F3B
  hgvsc: ENST00000589417.1:n.282A>G
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000586518
  gene symbol: H3F3B
  hgvsc: ENST00000586518.1:n.747A>G
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000467165
  ensembl transcript: ENST00000592643
  gene symbol: H3F3B
  hgvsc: ENST00000592643.1:c.128+21A>G
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000254810
  ensembl transcript: ENST00000254810
  gene symbol: H3F3B
  hgvsc: ENST00000254810.4:c.128+21A>G
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000465403
  ensembl transcript: ENST00000586270
  gene symbol: H3F3B
  hgvsc: ENST00000586270.1:c.128+21A>G
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000468714
  ensembl transcript: ENST00000587560
  gene symbol: H3F3B
  hgvsc: ENST00000587560.1:c.128+21A>G
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000466663
  ensembl transcript: ENST00000591890
  gene symbol: H3F3B
  hgvsc: ENST00000591890.1:c.128+21A>G
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000466020
  ensembl transcript: ENST00000586607
  gene symbol: H3F3B
  hgvsc: ENST00000586607.1:c.128+21A>G
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000468484
  ensembl transcript: ENST00000587171
  gene symbol: H3F3B
  hgvsc: ENST00000587171.1:c.128+21A>G
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000465813
  ensembl transcript: ENST00000589599
  gene symbol: H3F3B
  hgvsc: ENST00000589599.1:c.128+21A>G
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000593254
  gene symbol: H3F3B
  hgvsc: ENST00000593254.1:n.118-144A>G
  variant of: http://identifiers.org/hgnc/4765
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15994
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6570
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1109
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1769
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23917
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5353
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: South Asian
population: Other
population: East Asian
population: African
reference allele: T
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD

17-73775109-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73775109
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 73775109
    reference: chr 17
allele count: 3
allele frequency: 2.565944780868316e-5
allele num: 116916
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000468484
  ensembl transcript: ENST00000587171
  gene symbol: H3F3B
  hgvsc: ENST00000587171.1:c.128+19C>T
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000466020
  ensembl transcript: ENST00000586607
  gene symbol: H3F3B
  hgvsc: ENST00000586607.1:c.128+19C>T
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000466663
  ensembl transcript: ENST00000591890
  gene symbol: H3F3B
  hgvsc: ENST00000591890.1:c.128+19C>T
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000589949
  gene symbol: H3F3B
  hgvsc: ENST00000589949.1:n.267C>T
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000589417
  gene symbol: H3F3B
  hgvsc: ENST00000589417.1:n.280C>T
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000467165
  ensembl transcript: ENST00000592643
  gene symbol: H3F3B
  hgvsc: ENST00000592643.1:c.128+19C>T
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000254810
  ensembl transcript: ENST00000254810
  gene symbol: H3F3B
  hgvsc: ENST00000254810.4:c.128+19C>T
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000586518
  gene symbol: H3F3B
  hgvsc: ENST00000586518.1:n.745C>T
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000468714
  ensembl transcript: ENST00000587560
  gene symbol: H3F3B
  hgvsc: ENST00000587560.1:c.128+19C>T
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000465813
  ensembl transcript: ENST00000589599
  gene symbol: H3F3B
  hgvsc: ENST00000589599.1:c.128+19C>T
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000465403
  ensembl transcript: ENST00000586270
  gene symbol: H3F3B
  hgvsc: ENST00000586270.1:c.128+19C>T
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000593254
  gene symbol: H3F3B
  hgvsc: ENST00000593254.1:n.118-146C>T
  variant of: http://identifiers.org/hgnc/4765
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16021
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6497
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1790
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4993
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23560
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5631
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1109
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Latino
population: East Asian
reference allele: G
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ

17-73775111-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73775111
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 73775111
    reference: chr 17
allele count: 1
allele frequency: 8.573829243616784e-6
allele num: 116634
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000586518
  gene symbol: H3F3B
  hgvsc: ENST00000586518.1:n.743A>T
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000468714
  ensembl transcript: ENST00000587560
  gene symbol: H3F3B
  hgvsc: ENST00000587560.1:c.128+17A>T
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000466020
  ensembl transcript: ENST00000586607
  gene symbol: H3F3B
  hgvsc: ENST00000586607.1:c.128+17A>T
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000465813
  ensembl transcript: ENST00000589599
  gene symbol: H3F3B
  hgvsc: ENST00000589599.1:c.128+17A>T
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000468484
  ensembl transcript: ENST00000587171
  gene symbol: H3F3B
  hgvsc: ENST00000587171.1:c.128+17A>T
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000465403
  ensembl transcript: ENST00000586270
  gene symbol: H3F3B
  hgvsc: ENST00000586270.1:c.128+17A>T
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000589417
  gene symbol: H3F3B
  hgvsc: ENST00000589417.1:n.278A>T
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000467165
  ensembl transcript: ENST00000592643
  gene symbol: H3F3B
  hgvsc: ENST00000592643.1:c.128+17A>T
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000254810
  ensembl transcript: ENST00000254810
  gene symbol: H3F3B
  hgvsc: ENST00000254810.4:c.128+17A>T
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000589949
  gene symbol: H3F3B
  hgvsc: ENST00000589949.1:n.265A>T
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000466663
  ensembl transcript: ENST00000591890
  gene symbol: H3F3B
  hgvsc: ENST00000591890.1:c.128+17A>T
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000593254
  gene symbol: H3F3B
  hgvsc: ENST00000593254.1:n.118-148A>T
  variant of: http://identifiers.org/hgnc/4765
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6090
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5177
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1117
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1843
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6333
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15994
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23050
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: African
population: South Asian
population: Latino
population: Other
population: East Asian
population: European (Non-Finnish)
reference allele: T
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: MQ

17-73775111-T-TC
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73775111
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 73775112
    reference: chr 17
allele count: 1
allele frequency: 8.573829243616784e-6
allele num: 116634
alternate allele: TC
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000465813
  ensembl transcript: ENST00000589599
  gene symbol: H3F3B
  hgvsc: ENST00000589599.1:c.128+16dupG
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000589417
  gene symbol: H3F3B
  hgvsc: ENST00000589417.1:n.277dupG
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000468484
  ensembl transcript: ENST00000587171
  gene symbol: H3F3B
  hgvsc: ENST00000587171.1:c.128+16dupG
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000589949
  gene symbol: H3F3B
  hgvsc: ENST00000589949.1:n.264dupG
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000466663
  ensembl transcript: ENST00000591890
  gene symbol: H3F3B
  hgvsc: ENST00000591890.1:c.128+16dupG
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000254810
  ensembl transcript: ENST00000254810
  gene symbol: H3F3B
  hgvsc: ENST00000254810.4:c.128+16dupG
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000468714
  ensembl transcript: ENST00000587560
  gene symbol: H3F3B
  hgvsc: ENST00000587560.1:c.128+16dupG
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000586518
  gene symbol: H3F3B
  hgvsc: ENST00000586518.1:n.742dupG
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000593254
  gene symbol: H3F3B
  hgvsc: ENST00000593254.1:n.118-149dupG
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000466020
  ensembl transcript: ENST00000586607
  gene symbol: H3F3B
  hgvsc: ENST00000586607.1:c.128+16dupG
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000465403
  ensembl transcript: ENST00000586270
  gene symbol: H3F3B
  hgvsc: ENST00000586270.1:c.128+16dupG
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000467165
  ensembl transcript: ENST00000592643
  gene symbol: H3F3B
  hgvsc: ENST00000592643.1:c.128+16dupG
  variant of: http://identifiers.org/hgnc/4765
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1117
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5177
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1843
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23050
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6090
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6333
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15994
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: East Asian
population: African
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: DP

17-73775111-TC-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73775111
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 73775110
    reference: chr 17
allele count: 1
allele frequency: 8.573829243616784e-6
allele num: 116634
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000468484
  ensembl transcript: ENST00000587171
  gene symbol: H3F3B
  hgvsc: ENST00000587171.1:c.128+16delG
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000466663
  ensembl transcript: ENST00000591890
  gene symbol: H3F3B
  hgvsc: ENST00000591890.1:c.128+16delG
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000589949
  gene symbol: H3F3B
  hgvsc: ENST00000589949.1:n.264delG
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000465403
  ensembl transcript: ENST00000586270
  gene symbol: H3F3B
  hgvsc: ENST00000586270.1:c.128+16delG
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000586518
  gene symbol: H3F3B
  hgvsc: ENST00000586518.1:n.742delG
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000468714
  ensembl transcript: ENST00000587560
  gene symbol: H3F3B
  hgvsc: ENST00000587560.1:c.128+16delG
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000254810
  ensembl transcript: ENST00000254810
  gene symbol: H3F3B
  hgvsc: ENST00000254810.4:c.128+16delG
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000467165
  ensembl transcript: ENST00000592643
  gene symbol: H3F3B
  hgvsc: ENST00000592643.1:c.128+16delG
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000593254
  gene symbol: H3F3B
  hgvsc: ENST00000593254.1:n.118-149delG
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000466020
  ensembl transcript: ENST00000586607
  gene symbol: H3F3B
  hgvsc: ENST00000586607.1:c.128+16delG
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000465813
  ensembl transcript: ENST00000589599
  gene symbol: H3F3B
  hgvsc: ENST00000589599.1:c.128+16delG
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000589417
  gene symbol: H3F3B
  hgvsc: ENST00000589417.1:n.277delG
  variant of: http://identifiers.org/hgnc/4765
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1117
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6333
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15994
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6090
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5177
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1843
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Latino
population: East Asian
population: European (Non-Finnish)
population: African
population: Other
reference allele: TC
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum

17-73775113-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73775113
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 73775113
    reference: chr 17
allele count: 4
allele frequency: 3.432887058015791e-5
allele num: 116520
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000466020
  ensembl transcript: ENST00000586607
  gene symbol: H3F3B
  hgvsc: ENST00000586607.1:c.128+15G>C
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000254810
  ensembl transcript: ENST00000254810
  gene symbol: H3F3B
  hgvsc: ENST00000254810.4:c.128+15G>C
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000468714
  ensembl transcript: ENST00000587560
  gene symbol: H3F3B
  hgvsc: ENST00000587560.1:c.128+15G>C
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000467165
  ensembl transcript: ENST00000592643
  gene symbol: H3F3B
  hgvsc: ENST00000592643.1:c.128+15G>C
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000593254
  gene symbol: H3F3B
  hgvsc: ENST00000593254.1:n.118-150G>C
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000468484
  ensembl transcript: ENST00000587171
  gene symbol: H3F3B
  hgvsc: ENST00000587171.1:c.128+15G>C
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000466663
  ensembl transcript: ENST00000591890
  gene symbol: H3F3B
  hgvsc: ENST00000591890.1:c.128+15G>C
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000465813
  ensembl transcript: ENST00000589599
  gene symbol: H3F3B
  hgvsc: ENST00000589599.1:c.128+15G>C
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000465403
  ensembl transcript: ENST00000586270
  gene symbol: H3F3B
  hgvsc: ENST00000586270.1:c.128+15G>C
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000589417
  gene symbol: H3F3B
  hgvsc: ENST00000589417.1:n.276G>C
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000586518
  gene symbol: H3F3B
  hgvsc: ENST00000586518.1:n.741G>C
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000589949
  gene symbol: H3F3B
  hgvsc: ENST00000589949.1:n.263G>C
  variant of: http://identifiers.org/hgnc/4765
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5315
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1085
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6364
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16024
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6248
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1911
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22656
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 377
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: African
population: Latino
population: Other
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum

17-73775117-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73775117
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 73775117
    reference: chr 17
allele count: 1
allele frequency: 8.592394012819852e-6
allele num: 116382
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000466663
  ensembl transcript: ENST00000591890
  gene symbol: H3F3B
  hgvsc: ENST00000591890.1:c.128+11C>T
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000593254
  gene symbol: H3F3B
  hgvsc: ENST00000593254.1:n.118-154C>T
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000589949
  gene symbol: H3F3B
  hgvsc: ENST00000589949.1:n.259C>T
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000465813
  ensembl transcript: ENST00000589599
  gene symbol: H3F3B
  hgvsc: ENST00000589599.1:c.128+11C>T
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000468714
  ensembl transcript: ENST00000587560
  gene symbol: H3F3B
  hgvsc: ENST00000587560.1:c.128+11C>T
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000589417
  gene symbol: H3F3B
  hgvsc: ENST00000589417.1:n.272C>T
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000467165
  ensembl transcript: ENST00000592643
  gene symbol: H3F3B
  hgvsc: ENST00000592643.1:c.128+11C>T
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000254810
  ensembl transcript: ENST00000254810
  gene symbol: H3F3B
  hgvsc: ENST00000254810.4:c.128+11C>T
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000586518
  gene symbol: H3F3B
  hgvsc: ENST00000586518.1:n.737C>T
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000466020
  ensembl transcript: ENST00000586607
  gene symbol: H3F3B
  hgvsc: ENST00000586607.1:c.128+11C>T
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000465403
  ensembl transcript: ENST00000586270
  gene symbol: H3F3B
  hgvsc: ENST00000586270.1:c.128+11C>T
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000468484
  ensembl transcript: ENST00000587171
  gene symbol: H3F3B
  hgvsc: ENST00000587171.1:c.128+11C>T
  variant of: http://identifiers.org/hgnc/4765
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 22254
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5937
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1976
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6344
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5406
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16648
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1058
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: East Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff

17-73775118-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73775118
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 73775118
    reference: chr 17
allele count: 8
allele frequency: 6.871907641561298e-5
allele num: 116416
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000467165
  ensembl transcript: ENST00000592643
  gene symbol: H3F3B
  hgvsc: ENST00000592643.1:c.128+10G>A
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000254810
  ensembl transcript: ENST00000254810
  gene symbol: H3F3B
  hgvsc: ENST00000254810.4:c.128+10G>A
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000468714
  ensembl transcript: ENST00000587560
  gene symbol: H3F3B
  hgvsc: ENST00000587560.1:c.128+10G>A
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000466020
  ensembl transcript: ENST00000586607
  gene symbol: H3F3B
  hgvsc: ENST00000586607.1:c.128+10G>A
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000593254
  gene symbol: H3F3B
  hgvsc: ENST00000593254.1:n.118-155G>A
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000589949
  gene symbol: H3F3B
  hgvsc: ENST00000589949.1:n.258G>A
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000465813
  ensembl transcript: ENST00000589599
  gene symbol: H3F3B
  hgvsc: ENST00000589599.1:c.128+10G>A
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000586518
  gene symbol: H3F3B
  hgvsc: ENST00000586518.1:n.736G>A
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000465403
  ensembl transcript: ENST00000586270
  gene symbol: H3F3B
  hgvsc: ENST00000586270.1:c.128+10G>A
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000466663
  ensembl transcript: ENST00000591890
  gene symbol: H3F3B
  hgvsc: ENST00000591890.1:c.128+10G>A
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000589417
  gene symbol: H3F3B
  hgvsc: ENST00000589417.1:n.271G>A
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000468484
  ensembl transcript: ENST00000587171
  gene symbol: H3F3B
  hgvsc: ENST00000587171.1:c.128+10G>A
  variant of: http://identifiers.org/hgnc/4765
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16724
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5466
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5859
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1047
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1997
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6469
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 342
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22061
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: Other
population: South Asian
population: East Asian
reference allele: C
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: DP

17-73775119-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73775119
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 73775119
    reference: chr 17
allele count: 2
allele frequency: 1.717534307747797e-5
allele num: 116446
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000466020
  ensembl transcript: ENST00000586607
  gene symbol: H3F3B
  hgvsc: ENST00000586607.1:c.128+9G>A
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000465403
  ensembl transcript: ENST00000586270
  gene symbol: H3F3B
  hgvsc: ENST00000586270.1:c.128+9G>A
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000589949
  gene symbol: H3F3B
  hgvsc: ENST00000589949.1:n.257G>A
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000467165
  ensembl transcript: ENST00000592643
  gene symbol: H3F3B
  hgvsc: ENST00000592643.1:c.128+9G>A
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000466663
  ensembl transcript: ENST00000591890
  gene symbol: H3F3B
  hgvsc: ENST00000591890.1:c.128+9G>A
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000468714
  ensembl transcript: ENST00000587560
  gene symbol: H3F3B
  hgvsc: ENST00000587560.1:c.128+9G>A
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000586518
  gene symbol: H3F3B
  hgvsc: ENST00000586518.1:n.735G>A
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000589417
  gene symbol: H3F3B
  hgvsc: ENST00000589417.1:n.270G>A
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000254810
  ensembl transcript: ENST00000254810
  gene symbol: H3F3B
  hgvsc: ENST00000254810.4:c.128+9G>A
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000593254
  gene symbol: H3F3B
  hgvsc: ENST00000593254.1:n.118-156G>A
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000465813
  ensembl transcript: ENST00000589599
  gene symbol: H3F3B
  hgvsc: ENST00000589599.1:c.128+9G>A
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000468484
  ensembl transcript: ENST00000587171
  gene symbol: H3F3B
  hgvsc: ENST00000587171.1:c.128+9G>A
  variant of: http://identifiers.org/hgnc/4765
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1045
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5477
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22109
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 341
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16829
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1998
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5818
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6349
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: European (Finnish)
population: East Asian
population: Other
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum

17-73775133-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73775133
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 73775133
    reference: chr 17
allele count: 1
allele frequency: 8.614303189015041e-6
allele num: 116086
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000593254
  gene symbol: H3F3B
  hgvsc: ENST00000593254.1:n.118-170C>T
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000468714
  ensembl transcript: ENST00000587560
  gene symbol: H3F3B
  hgvsc: ENST00000587560.1:c.123C>T
  hgvsp: ENST00000587560.1:c.123C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000467165
  ensembl transcript: ENST00000592643
  gene symbol: H3F3B
  hgvsc: ENST00000592643.1:c.123C>T
  hgvsp: ENST00000592643.1:c.123C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000465813
  ensembl transcript: ENST00000589599
  gene symbol: H3F3B
  hgvsc: ENST00000589599.1:c.123C>T
  hgvsp: ENST00000589599.1:c.123C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000466020
  ensembl transcript: ENST00000586607
  gene symbol: H3F3B
  hgvsc: ENST00000586607.1:c.123C>T
  hgvsp: ENST00000586607.1:c.123C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000465403
  ensembl transcript: ENST00000586270
  gene symbol: H3F3B
  hgvsc: ENST00000586270.1:c.123C>T
  hgvsp: ENST00000586270.1:c.123C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000468484
  ensembl transcript: ENST00000587171
  gene symbol: H3F3B
  hgvsc: ENST00000587171.1:c.123C>T
  hgvsp: ENST00000587171.1:c.123C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000466663
  ensembl transcript: ENST00000591890
  gene symbol: H3F3B
  hgvsc: ENST00000591890.1:c.123C>T
  hgvsp: ENST00000591890.1:c.123C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000589949
  gene symbol: H3F3B
  hgvsc: ENST00000589949.1:n.243C>T
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000254810
  ensembl transcript: ENST00000254810
  gene symbol: H3F3B
  hgvsc: ENST00000254810.4:c.123C>T
  hgvsp: ENST00000254810.4:c.123C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000586518
  gene symbol: H3F3B
  hgvsc: ENST00000586518.1:n.721C>T
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000589417
  gene symbol: H3F3B
  hgvsc: ENST00000589417.1:n.256C>T
  variant of: http://identifiers.org/hgnc/4765
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7087
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5214
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5825
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 342
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1013
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17970
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2212
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20319
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg41Arg
num of homozygotes: 0
population: Other
population: European (Finnish)
population: African
population: South Asian
population: East Asian
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: FS

17-73775136-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73775136
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 73775136
    reference: chr 17
allele count: 2
allele frequency: 1.723870433898188e-5
allele num: 116018
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000589417
  gene symbol: H3F3B
  hgvsc: ENST00000589417.1:n.253T>C
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000466663
  ensembl transcript: ENST00000591890
  gene symbol: H3F3B
  hgvsc: ENST00000591890.1:c.120T>C
  hgvsp: ENST00000591890.1:c.120T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000465813
  ensembl transcript: ENST00000589599
  gene symbol: H3F3B
  hgvsc: ENST00000589599.1:c.120T>C
  hgvsp: ENST00000589599.1:c.120T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000254810
  ensembl transcript: ENST00000254810
  gene symbol: H3F3B
  hgvsc: ENST00000254810.4:c.120T>C
  hgvsp: ENST00000254810.4:c.120T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000466020
  ensembl transcript: ENST00000586607
  gene symbol: H3F3B
  hgvsc: ENST00000586607.1:c.120T>C
  hgvsp: ENST00000586607.1:c.120T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000586518
  gene symbol: H3F3B
  hgvsc: ENST00000586518.1:n.718T>C
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000468714
  ensembl transcript: ENST00000587560
  gene symbol: H3F3B
  hgvsc: ENST00000587560.1:c.120T>C
  hgvsp: ENST00000587560.1:c.120T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000465403
  ensembl transcript: ENST00000586270
  gene symbol: H3F3B
  hgvsc: ENST00000586270.1:c.120T>C
  hgvsp: ENST00000586270.1:c.120T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000468484
  ensembl transcript: ENST00000587171
  gene symbol: H3F3B
  hgvsc: ENST00000587171.1:c.120T>C
  hgvsp: ENST00000587171.1:c.120T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000467165
  ensembl transcript: ENST00000592643
  gene symbol: H3F3B
  hgvsc: ENST00000592643.1:c.120T>C
  hgvsp: ENST00000592643.1:c.120T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000593254
  gene symbol: H3F3B
  hgvsc: ENST00000593254.1:n.118-173T>C
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000589949
  gene symbol: H3F3B
  hgvsc: ENST00000589949.1:n.240T>C
  variant of: http://identifiers.org/hgnc/4765
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5829
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2263
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18255
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20017
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 342
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5122
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1012
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.His40His
num of homozygotes: 0
population: East Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Latino
population: South Asian
reference allele: A
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: DP

17-73775148-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73775148
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 73775148
    reference: chr 17
allele count: 59
allele frequency: 5.113892452241445e-4
allele num: 115372
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000468484
  ensembl transcript: ENST00000587171
  gene symbol: H3F3B
  hgvsc: ENST00000587171.1:c.108G>C
  hgvsp: ENST00000587171.1:c.108G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000465813
  ensembl transcript: ENST00000589599
  gene symbol: H3F3B
  hgvsc: ENST00000589599.1:c.108G>C
  hgvsp: ENST00000589599.1:c.108G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000468714
  ensembl transcript: ENST00000587560
  gene symbol: H3F3B
  hgvsc: ENST00000587560.1:c.108G>C
  hgvsp: ENST00000587560.1:c.108G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000465403
  ensembl transcript: ENST00000586270
  gene symbol: H3F3B
  hgvsc: ENST00000586270.1:c.108G>C
  hgvsp: ENST00000586270.1:c.108G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000586518
  gene symbol: H3F3B
  hgvsc: ENST00000586518.1:n.706G>C
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000254810
  ensembl transcript: ENST00000254810
  gene symbol: H3F3B
  hgvsc: ENST00000254810.4:c.108G>C
  hgvsp: ENST00000254810.4:c.108G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000467165
  ensembl transcript: ENST00000592643
  gene symbol: H3F3B
  hgvsc: ENST00000592643.1:c.108G>C
  hgvsp: ENST00000592643.1:c.108G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000466663
  ensembl transcript: ENST00000591890
  gene symbol: H3F3B
  hgvsc: ENST00000591890.1:c.108G>C
  hgvsp: ENST00000591890.1:c.108G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000466020
  ensembl transcript: ENST00000586607
  gene symbol: H3F3B
  hgvsc: ENST00000586607.1:c.108G>C
  hgvsp: ENST00000586607.1:c.108G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000589417
  gene symbol: H3F3B
  hgvsc: ENST00000589417.1:n.241G>C
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000589949
  gene symbol: H3F3B
  hgvsc: ENST00000589949.1:n.228G>C
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000593254
  gene symbol: H3F3B
  hgvsc: ENST00000593254.1:n.118-185G>C
  variant of: http://identifiers.org/hgnc/4765
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 18835
  bin: 2.25e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 19088
  bin: 2.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5017
  bin: 3.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 2428
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5683
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 4.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 7566
  bin: 1.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 361
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1016
  bin: 3.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val36Val
num of homozygotes: 1
population: South Asian
population: East Asian
population: Other
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: African
reference allele: C
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: QD

http://identifiers.org/exac.variant/17-73775149-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73775149
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 73775149
    reference: chr 17
allele count: 122
allele frequency: 1.158044613194115e-3
allele num: 105350
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000468714
  ensembl transcript: ENST00000587560
  gene symbol: H3F3B
  hgvsc: ENST00000587560.1:c.107T>G
  hgvsp: ENSP00000468714.1:p.Val36Gly
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000465403
  ensembl transcript: ENST00000586270
  gene symbol: H3F3B
  hgvsc: ENST00000586270.1:c.107T>G
  hgvsp: ENSP00000465403.1:p.Val36Gly
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000466663
  ensembl transcript: ENST00000591890
  gene symbol: H3F3B
  hgvsc: ENST00000591890.1:c.107T>G
  hgvsp: ENSP00000466663.1:p.Val36Gly
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000465813
  ensembl transcript: ENST00000589599
  gene symbol: H3F3B
  hgvsc: ENST00000589599.1:c.107T>G
  hgvsp: ENSP00000465813.1:p.Val36Gly
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000467165
  ensembl transcript: ENST00000592643
  gene symbol: H3F3B
  hgvsc: ENST00000592643.1:c.107T>G
  hgvsp: ENSP00000467165.1:p.Val36Gly
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000589949
  gene symbol: H3F3B
  hgvsc: ENST00000589949.1:n.227T>G
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000468484
  ensembl transcript: ENST00000587171
  gene symbol: H3F3B
  hgvsc: ENST00000587171.1:c.107T>G
  hgvsp: ENSP00000468484.1:p.Val36Gly
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000254810
  ensembl transcript: ENST00000254810
  gene symbol: H3F3B
  hgvsc: ENST00000254810.4:c.107T>G
  hgvsp: ENSP00000254810.3:p.Val36Gly
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000593254
  gene symbol: H3F3B
  hgvsc: ENST00000593254.1:n.118-186T>G
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000466020
  ensembl transcript: ENST00000586607
  gene symbol: H3F3B
  hgvsc: ENST00000586607.1:c.107T>G
  hgvsp: ENSP00000466020.1:p.Val36Gly
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000589417
  gene symbol: H3F3B
  hgvsc: ENST00000589417.1:n.240T>G
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000586518
  gene symbol: H3F3B
  hgvsc: ENST00000586518.1:n.705T>G
  variant of: http://identifiers.org/hgnc/4765
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.95to100.00
genotype depth: GenotypeDepth
  all individuals: 2441
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 400
  bin: 4.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 18019
  bin: 2.75e1
  variant carriers: 28
genotype depth: GenotypeDepth
  all individuals: 5697
  bin: 1.25e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 4.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1130
  bin: 3.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 18518
  bin: 2.25e1
  variant carriers: 33
genotype depth: GenotypeDepth
  all individuals: 8634
  bin: 1.75e1
  variant carriers: 19
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5103
  bin: 3.25e1
  variant carriers: 21
genotype quality: GenotypeQuality
hgvs: p.Val36Gly
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: Other
population: South Asian
population: African
population: East Asian
population: European (Finnish)
reference allele: A
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: MQ

17-73775151-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73775151
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 73775151
    reference: chr 17
allele count: 1
allele frequency: 8.646629543803825e-6
allele num: 115652
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000589949
  gene symbol: H3F3B
  hgvsc: ENST00000589949.1:n.225G>A
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000466663
  ensembl transcript: ENST00000591890
  gene symbol: H3F3B
  hgvsc: ENST00000591890.1:c.105G>A
  hgvsp: ENST00000591890.1:c.105G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000468714
  ensembl transcript: ENST00000587560
  gene symbol: H3F3B
  hgvsc: ENST00000587560.1:c.105G>A
  hgvsp: ENST00000587560.1:c.105G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000467165
  ensembl transcript: ENST00000592643
  gene symbol: H3F3B
  hgvsc: ENST00000592643.1:c.105G>A
  hgvsp: ENST00000592643.1:c.105G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000466020
  ensembl transcript: ENST00000586607
  gene symbol: H3F3B
  hgvsc: ENST00000586607.1:c.105G>A
  hgvsp: ENST00000586607.1:c.105G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000593254
  gene symbol: H3F3B
  hgvsc: ENST00000593254.1:n.118-188G>A
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000465403
  ensembl transcript: ENST00000586270
  gene symbol: H3F3B
  hgvsc: ENST00000586270.1:c.105G>A
  hgvsp: ENST00000586270.1:c.105G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000589417
  gene symbol: H3F3B
  hgvsc: ENST00000589417.1:n.238G>A
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000254810
  ensembl transcript: ENST00000254810
  gene symbol: H3F3B
  hgvsc: ENST00000254810.4:c.105G>A
  hgvsp: ENST00000254810.4:c.105G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000468484
  ensembl transcript: ENST00000587171
  gene symbol: H3F3B
  hgvsc: ENST00000587171.1:c.105G>A
  hgvsp: ENST00000587171.1:c.105G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000586518
  gene symbol: H3F3B
  hgvsc: ENST00000586518.1:n.703G>A
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000465813
  ensembl transcript: ENST00000589599
  gene symbol: H3F3B
  hgvsc: ENST00000589599.1:c.105G>A
  hgvsp: ENST00000589599.1:c.105G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4765
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5264
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18159
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4981
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23402
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2411
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly35Gly
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Latino
population: African
population: Other
population: European (Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD

17-73775154-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73775154
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 73775154
    reference: chr 17
allele count: 1
allele frequency: 8.638413296245746e-6
allele num: 115762
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000589949
  gene symbol: H3F3B
  hgvsc: ENST00000589949.1:n.222C>T
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000254810
  ensembl transcript: ENST00000254810
  gene symbol: H3F3B
  hgvsc: ENST00000254810.4:c.102C>T
  hgvsp: ENST00000254810.4:c.102C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000467165
  ensembl transcript: ENST00000592643
  gene symbol: H3F3B
  hgvsc: ENST00000592643.1:c.102C>T
  hgvsp: ENST00000592643.1:c.102C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000466020
  ensembl transcript: ENST00000586607
  gene symbol: H3F3B
  hgvsc: ENST00000586607.1:c.102C>T
  hgvsp: ENST00000586607.1:c.102C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000593254
  gene symbol: H3F3B
  hgvsc: ENST00000593254.1:n.118-191C>T
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000468714
  ensembl transcript: ENST00000587560
  gene symbol: H3F3B
  hgvsc: ENST00000587560.1:c.102C>T
  hgvsp: ENST00000587560.1:c.102C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000465813
  ensembl transcript: ENST00000589599
  gene symbol: H3F3B
  hgvsc: ENST00000589599.1:c.102C>T
  hgvsp: ENST00000589599.1:c.102C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000466663
  ensembl transcript: ENST00000591890
  gene symbol: H3F3B
  hgvsc: ENST00000591890.1:c.102C>T
  hgvsp: ENST00000591890.1:c.102C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000589417
  gene symbol: H3F3B
  hgvsc: ENST00000589417.1:n.235C>T
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000468484
  ensembl transcript: ENST00000587171
  gene symbol: H3F3B
  hgvsc: ENST00000587171.1:c.102C>T
  hgvsp: ENST00000587171.1:c.102C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000586518
  gene symbol: H3F3B
  hgvsc: ENST00000586518.1:n.700C>T
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000465403
  ensembl transcript: ENST00000586270
  gene symbol: H3F3B
  hgvsc: ENST00000586270.1:c.102C>T
  hgvsp: ENST00000586270.1:c.102C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4765
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19220
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 600
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23689
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4567
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2431
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5291
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly34Gly
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: African
population: Latino
population: Other
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: DP

17-73775157-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73775157
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 73775157
    reference: chr 17
allele count: 340
allele frequency: 2.936451729915534e-3
allele num: 115786
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000467165
  ensembl transcript: ENST00000592643
  gene symbol: H3F3B
  hgvsc: ENST00000592643.1:c.99C>T
  hgvsp: ENST00000592643.1:c.99C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000466020
  ensembl transcript: ENST00000586607
  gene symbol: H3F3B
  hgvsc: ENST00000586607.1:c.99C>T
  hgvsp: ENST00000586607.1:c.99C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000465813
  ensembl transcript: ENST00000589599
  gene symbol: H3F3B
  hgvsc: ENST00000589599.1:c.99C>T
  hgvsp: ENST00000589599.1:c.99C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000593254
  gene symbol: H3F3B
  hgvsc: ENST00000593254.1:n.118-194C>T
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000465403
  ensembl transcript: ENST00000586270
  gene symbol: H3F3B
  hgvsc: ENST00000586270.1:c.99C>T
  hgvsp: ENST00000586270.1:c.99C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000586518
  gene symbol: H3F3B
  hgvsc: ENST00000586518.1:n.697C>T
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000589417
  gene symbol: H3F3B
  hgvsc: ENST00000589417.1:n.232C>T
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000468484
  ensembl transcript: ENST00000587171
  gene symbol: H3F3B
  hgvsc: ENST00000587171.1:c.99C>T
  hgvsp: ENST00000587171.1:c.99C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000254810
  ensembl transcript: ENST00000254810
  gene symbol: H3F3B
  hgvsc: ENST00000254810.4:c.99C>T
  hgvsp: ENST00000254810.4:c.99C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000466663
  ensembl transcript: ENST00000591890
  gene symbol: H3F3B
  hgvsc: ENST00000591890.1:c.99C>T
  hgvsp: ENST00000591890.1:c.99C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000589949
  gene symbol: H3F3B
  hgvsc: ENST00000589949.1:n.219C>T
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000468714
  ensembl transcript: ENST00000587560
  gene symbol: H3F3B
  hgvsc: ENST00000587560.1:c.99C>T
  hgvsp: ENST00000587560.1:c.99C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4765
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 608
  bin: 3.75e1
  variant carriers: 36
genotype depth: GenotypeDepth
  all individuals: 3588
  bin: 1.75e1
  variant carriers: 32
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 6.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 20027
  bin: 2.25e1
  variant carriers: 45
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 4.75e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2417
  bin: 7.5e0
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 23827
  bin: 2.75e1
  variant carriers: 61
genotype depth: GenotypeDepth
  all individuals: 5325
  bin: 3.25e1
  variant carriers: 48
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 5.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 4198
  bin: 1.25e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 5.25e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 9.75e1
  variant carriers: 19
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 4.25e1
  variant carriers: 26
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
hgvs: p.Thr33Thr
num of homozygotes: 5
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: African
population: Latino
population: Other
population: European (Finnish)
reference allele: G
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD

17-73775163-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73775163
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 73775163
    reference: chr 17
allele count: 4
allele frequency: 3.448454230391227e-5
allele num: 115994
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000589949
  gene symbol: H3F3B
  hgvsc: ENST00000589949.1:n.213C>G
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000589417
  gene symbol: H3F3B
  hgvsc: ENST00000589417.1:n.226C>G
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000593254
  gene symbol: H3F3B
  hgvsc: ENST00000593254.1:n.118-200C>G
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000465813
  ensembl transcript: ENST00000589599
  gene symbol: H3F3B
  hgvsc: ENST00000589599.1:c.93C>G
  hgvsp: ENST00000589599.1:c.93C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000466663
  ensembl transcript: ENST00000591890
  gene symbol: H3F3B
  hgvsc: ENST00000591890.1:c.93C>G
  hgvsp: ENST00000591890.1:c.93C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000465403
  ensembl transcript: ENST00000586270
  gene symbol: H3F3B
  hgvsc: ENST00000586270.1:c.93C>G
  hgvsp: ENST00000586270.1:c.93C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000467165
  ensembl transcript: ENST00000592643
  gene symbol: H3F3B
  hgvsc: ENST00000592643.1:c.93C>G
  hgvsp: ENST00000592643.1:c.93C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000468714
  ensembl transcript: ENST00000587560
  gene symbol: H3F3B
  hgvsc: ENST00000587560.1:c.93C>G
  hgvsp: ENST00000587560.1:c.93C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000254810
  ensembl transcript: ENST00000254810
  gene symbol: H3F3B
  hgvsc: ENST00000254810.4:c.93C>G
  hgvsp: ENST00000254810.4:c.93C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000466020
  ensembl transcript: ENST00000586607
  gene symbol: H3F3B
  hgvsc: ENST00000586607.1:c.93C>G
  hgvsp: ENST00000586607.1:c.93C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000586518
  gene symbol: H3F3B
  hgvsc: ENST00000586518.1:n.691C>G
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000468484
  ensembl transcript: ENST00000587171
  gene symbol: H3F3B
  hgvsc: ENST00000587171.1:c.93C>G
  hgvsp: ENST00000587171.1:c.93C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/4765
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 577
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5221
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3647
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21205
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2740
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2399
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro31Pro
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: South Asian
population: Latino
population: European (Finnish)
population: Other
population: East Asian
reference allele: G
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: QD

17-73775169-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73775169
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 73775169
    reference: chr 17
allele count: 1
allele frequency: 8.624555835374478e-6
allele num: 115948
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000586518
  gene symbol: H3F3B
  hgvsc: ENST00000586518.1:n.685C>T
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000465403
  ensembl transcript: ENST00000586270
  gene symbol: H3F3B
  hgvsc: ENST00000586270.1:c.87C>T
  hgvsp: ENST00000586270.1:c.87C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000593254
  gene symbol: H3F3B
  hgvsc: ENST00000593254.1:n.118-206C>T
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000465813
  ensembl transcript: ENST00000589599
  gene symbol: H3F3B
  hgvsc: ENST00000589599.1:c.87C>T
  hgvsp: ENST00000589599.1:c.87C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000589417
  gene symbol: H3F3B
  hgvsc: ENST00000589417.1:n.220C>T
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000467165
  ensembl transcript: ENST00000592643
  gene symbol: H3F3B
  hgvsc: ENST00000592643.1:c.87C>T
  hgvsp: ENST00000592643.1:c.87C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000254810
  ensembl transcript: ENST00000254810
  gene symbol: H3F3B
  hgvsc: ENST00000254810.4:c.87C>T
  hgvsp: ENST00000254810.4:c.87C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000468484
  ensembl transcript: ENST00000587171
  gene symbol: H3F3B
  hgvsc: ENST00000587171.1:c.87C>T
  hgvsp: ENST00000587171.1:c.87C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000466020
  ensembl transcript: ENST00000586607
  gene symbol: H3F3B
  hgvsc: ENST00000586607.1:c.87C>T
  hgvsp: ENST00000586607.1:c.87C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000466663
  ensembl transcript: ENST00000591890
  gene symbol: H3F3B
  hgvsc: ENST00000591890.1:c.87C>T
  hgvsp: ENST00000591890.1:c.87C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000468714
  ensembl transcript: ENST00000587560
  gene symbol: H3F3B
  hgvsc: ENST00000587560.1:c.87C>T
  hgvsp: ENST00000587560.1:c.87C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000589949
  gene symbol: H3F3B
  hgvsc: ENST00000589949.1:n.207C>T
  variant of: http://identifiers.org/hgnc/4765
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24693
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3331
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 569
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5297
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2397
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser29Ser
num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: European (Finnish)
population: Other
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: MQRankSum

17-73775175-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73775175
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 73775175
    reference: chr 17
allele count: 3
allele frequency: 2.584958985317433e-5
allele num: 116056
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000465403
  ensembl transcript: ENST00000586270
  gene symbol: H3F3B
  hgvsc: ENST00000586270.1:c.81G>A
  hgvsp: ENST00000586270.1:c.81G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000468714
  ensembl transcript: ENST00000587560
  gene symbol: H3F3B
  hgvsc: ENST00000587560.1:c.81G>A
  hgvsp: ENST00000587560.1:c.81G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000467165
  ensembl transcript: ENST00000592643
  gene symbol: H3F3B
  hgvsc: ENST00000592643.1:c.81G>A
  hgvsp: ENST00000592643.1:c.81G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000589949
  gene symbol: H3F3B
  hgvsc: ENST00000589949.1:n.201G>A
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000589417
  gene symbol: H3F3B
  hgvsc: ENST00000589417.1:n.214G>A
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000586518
  gene symbol: H3F3B
  hgvsc: ENST00000586518.1:n.679G>A
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000593254
  gene symbol: H3F3B
  hgvsc: ENST00000593254.1:n.118-212G>A
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000254810
  ensembl transcript: ENST00000254810
  gene symbol: H3F3B
  hgvsc: ENST00000254810.4:c.81G>A
  hgvsp: ENST00000254810.4:c.81G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000466663
  ensembl transcript: ENST00000591890
  gene symbol: H3F3B
  hgvsc: ENST00000591890.1:c.81G>A
  hgvsp: ENST00000591890.1:c.81G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000468484
  ensembl transcript: ENST00000587171
  gene symbol: H3F3B
  hgvsc: ENST00000587171.1:c.81G>A
  hgvsp: ENST00000587171.1:c.81G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000465813
  ensembl transcript: ENST00000589599
  gene symbol: H3F3B
  hgvsc: ENST00000589599.1:c.81G>A
  hgvsp: ENST00000589599.1:c.81G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000466020
  ensembl transcript: ENST00000586607
  gene symbol: H3F3B
  hgvsc: ENST00000586607.1:c.81G>A
  hgvsp: ENST00000586607.1:c.81G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4765
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5285
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 560
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2393
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 21925
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1930
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25020
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3022
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg27Arg
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: South Asian
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP

17-73775178-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73775178
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 73775178
    reference: chr 17
allele count: 6
allele frequency: 5.172235440157236e-5
allele num: 116004
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000465813
  ensembl transcript: ENST00000589599
  gene symbol: H3F3B
  hgvsc: ENST00000589599.1:c.78C>T
  hgvsp: ENST00000589599.1:c.78C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000254810
  ensembl transcript: ENST00000254810
  gene symbol: H3F3B
  hgvsc: ENST00000254810.4:c.78C>T
  hgvsp: ENST00000254810.4:c.78C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000468484
  ensembl transcript: ENST00000587171
  gene symbol: H3F3B
  hgvsc: ENST00000587171.1:c.78C>T
  hgvsp: ENST00000587171.1:c.78C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000465403
  ensembl transcript: ENST00000586270
  gene symbol: H3F3B
  hgvsc: ENST00000586270.1:c.78C>T
  hgvsp: ENST00000586270.1:c.78C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000589949
  gene symbol: H3F3B
  hgvsc: ENST00000589949.1:n.198C>T
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000589417
  gene symbol: H3F3B
  hgvsc: ENST00000589417.1:n.211C>T
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000466020
  ensembl transcript: ENST00000586607
  gene symbol: H3F3B
  hgvsc: ENST00000586607.1:c.78C>T
  hgvsp: ENST00000586607.1:c.78C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000467165
  ensembl transcript: ENST00000592643
  gene symbol: H3F3B
  hgvsc: ENST00000592643.1:c.78C>T
  hgvsp: ENST00000592643.1:c.78C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000468714
  ensembl transcript: ENST00000587560
  gene symbol: H3F3B
  hgvsc: ENST00000587560.1:c.78C>T
  hgvsp: ENST00000587560.1:c.78C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000466663
  ensembl transcript: ENST00000591890
  gene symbol: H3F3B
  hgvsc: ENST00000591890.1:c.78C>T
  hgvsp: ENST00000591890.1:c.78C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000586518
  gene symbol: H3F3B
  hgvsc: ENST00000586518.1:n.676C>T
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000593254
  gene symbol: H3F3B
  hgvsc: ENST00000593254.1:n.118-215C>T
  variant of: http://identifiers.org/hgnc/4765
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2927
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2426
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 25067
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 568
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22005
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1836
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 4.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Ala26Ala
num of homozygotes: 0
population: Latino
population: African
population: European (Finnish)
population: South Asian
population: Other
population: European (Non-Finnish)
population: East Asian
reference allele: G
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: QD

17-73775181-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73775181
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 73775181
    reference: chr 17
allele count: 3
allele frequency: 2.589823719332171e-5
allele num: 115838
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000466020
  ensembl transcript: ENST00000586607
  gene symbol: H3F3B
  hgvsc: ENST00000586607.1:c.75C>T
  hgvsp: ENST00000586607.1:c.75C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000465813
  ensembl transcript: ENST00000589599
  gene symbol: H3F3B
  hgvsc: ENST00000589599.1:c.75C>T
  hgvsp: ENST00000589599.1:c.75C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000586518
  gene symbol: H3F3B
  hgvsc: ENST00000586518.1:n.673C>T
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000589949
  gene symbol: H3F3B
  hgvsc: ENST00000589949.1:n.195C>T
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000465403
  ensembl transcript: ENST00000586270
  gene symbol: H3F3B
  hgvsc: ENST00000586270.1:c.75C>T
  hgvsp: ENST00000586270.1:c.75C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000593254
  gene symbol: H3F3B
  hgvsc: ENST00000593254.1:n.118-218C>T
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000467165
  ensembl transcript: ENST00000592643
  gene symbol: H3F3B
  hgvsc: ENST00000592643.1:c.75C>T
  hgvsp: ENST00000592643.1:c.75C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000468714
  ensembl transcript: ENST00000587560
  gene symbol: H3F3B
  hgvsc: ENST00000587560.1:c.75C>T
  hgvsp: ENST00000587560.1:c.75C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000466663
  ensembl transcript: ENST00000591890
  gene symbol: H3F3B
  hgvsc: ENST00000591890.1:c.75C>T
  hgvsp: ENST00000591890.1:c.75C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000589417
  gene symbol: H3F3B
  hgvsc: ENST00000589417.1:n.208C>T
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000468484
  ensembl transcript: ENST00000587171
  gene symbol: H3F3B
  hgvsc: ENST00000587171.1:c.75C>T
  hgvsp: ENST00000587171.1:c.75C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000254810
  ensembl transcript: ENST00000254810
  gene symbol: H3F3B
  hgvsc: ENST00000254810.4:c.75C>T
  hgvsp: ENST00000254810.4:c.75C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4765
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22035
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2871
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1719
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5288
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2505
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 555
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala25Ala
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Finnish)
population: African
population: Other
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum

17-73775181-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73775181
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 73775181
    reference: chr 17
allele count: 1
allele frequency: 8.632745731107236e-6
allele num: 115838
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000254810
  ensembl transcript: ENST00000254810
  gene symbol: H3F3B
  hgvsc: ENST00000254810.4:c.75C>G
  hgvsp: ENST00000254810.4:c.75C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000593254
  gene symbol: H3F3B
  hgvsc: ENST00000593254.1:n.118-218C>G
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000465813
  ensembl transcript: ENST00000589599
  gene symbol: H3F3B
  hgvsc: ENST00000589599.1:c.75C>G
  hgvsp: ENST00000589599.1:c.75C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000465403
  ensembl transcript: ENST00000586270
  gene symbol: H3F3B
  hgvsc: ENST00000586270.1:c.75C>G
  hgvsp: ENST00000586270.1:c.75C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000468714
  ensembl transcript: ENST00000587560
  gene symbol: H3F3B
  hgvsc: ENST00000587560.1:c.75C>G
  hgvsp: ENST00000587560.1:c.75C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000467165
  ensembl transcript: ENST00000592643
  gene symbol: H3F3B
  hgvsc: ENST00000592643.1:c.75C>G
  hgvsp: ENST00000592643.1:c.75C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000589949
  gene symbol: H3F3B
  hgvsc: ENST00000589949.1:n.195C>G
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000468484
  ensembl transcript: ENST00000587171
  gene symbol: H3F3B
  hgvsc: ENST00000587171.1:c.75C>G
  hgvsp: ENST00000587171.1:c.75C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000466020
  ensembl transcript: ENST00000586607
  gene symbol: H3F3B
  hgvsc: ENST00000586607.1:c.75C>G
  hgvsp: ENST00000586607.1:c.75C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000466663
  ensembl transcript: ENST00000591890
  gene symbol: H3F3B
  hgvsc: ENST00000591890.1:c.75C>G
  hgvsp: ENST00000591890.1:c.75C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000589417
  gene symbol: H3F3B
  hgvsc: ENST00000589417.1:n.208C>G
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000586518
  gene symbol: H3F3B
  hgvsc: ENST00000586518.1:n.673C>G
  variant of: http://identifiers.org/hgnc/4765
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 22035
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25156
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2505
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2871
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1719
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5288
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala25Ala
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: East Asian
population: South Asian
population: Other
population: African
population: European (Non-Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum

17-73775190-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73775190
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 73775190
    reference: chr 17
allele count: 1
allele frequency: 8.640503222907702e-6
allele num: 115734
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000465403
  ensembl transcript: ENST00000586270
  gene symbol: H3F3B
  hgvsc: ENST00000586270.1:c.66C>T
  hgvsp: ENST00000586270.1:c.66C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000468714
  ensembl transcript: ENST00000587560
  gene symbol: H3F3B
  hgvsc: ENST00000587560.1:c.66C>T
  hgvsp: ENST00000587560.1:c.66C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000466663
  ensembl transcript: ENST00000591890
  gene symbol: H3F3B
  hgvsc: ENST00000591890.1:c.66C>T
  hgvsp: ENST00000591890.1:c.66C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000586518
  gene symbol: H3F3B
  hgvsc: ENST00000586518.1:n.664C>T
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000589417
  gene symbol: H3F3B
  hgvsc: ENST00000589417.1:n.199C>T
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000589949
  gene symbol: H3F3B
  hgvsc: ENST00000589949.1:n.186C>T
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000465813
  ensembl transcript: ENST00000589599
  gene symbol: H3F3B
  hgvsc: ENST00000589599.1:c.66C>T
  hgvsp: ENST00000589599.1:c.66C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000254810
  ensembl transcript: ENST00000254810
  gene symbol: H3F3B
  hgvsc: ENST00000254810.4:c.66C>T
  hgvsp: ENST00000254810.4:c.66C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000593254
  gene symbol: H3F3B
  hgvsc: ENST00000593254.1:n.118-227C>T
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000467165
  ensembl transcript: ENST00000592643
  gene symbol: H3F3B
  hgvsc: ENST00000592643.1:c.66C>T
  hgvsp: ENST00000592643.1:c.66C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000466020
  ensembl transcript: ENST00000586607
  gene symbol: H3F3B
  hgvsc: ENST00000586607.1:c.66C>T
  hgvsp: ENST00000586607.1:c.66C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000468484
  ensembl transcript: ENST00000587171
  gene symbol: H3F3B
  hgvsc: ENST00000587171.1:c.66C>T
  hgvsp: ENST00000587171.1:c.66C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4765
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5282
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22463
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25415
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 550
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1257
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2575
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala22Ala
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Latino
population: African
population: European (Finnish)
population: Other
population: South Asian
reference allele: G
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP

17-73775193-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73775193
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 73775193
    reference: chr 17
allele count: 2
allele frequency: 1.730522964039733e-5
allele num: 115572
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000589417
  gene symbol: H3F3B
  hgvsc: ENST00000589417.1:n.196G>A
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000465813
  ensembl transcript: ENST00000589599
  gene symbol: H3F3B
  hgvsc: ENST00000589599.1:c.63G>A
  hgvsp: ENST00000589599.1:c.63G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000465403
  ensembl transcript: ENST00000586270
  gene symbol: H3F3B
  hgvsc: ENST00000586270.1:c.63G>A
  hgvsp: ENST00000586270.1:c.63G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000254810
  ensembl transcript: ENST00000254810
  gene symbol: H3F3B
  hgvsc: ENST00000254810.4:c.63G>A
  hgvsp: ENST00000254810.4:c.63G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000593254
  gene symbol: H3F3B
  hgvsc: ENST00000593254.1:n.118-230G>A
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000467165
  ensembl transcript: ENST00000592643
  gene symbol: H3F3B
  hgvsc: ENST00000592643.1:c.63G>A
  hgvsp: ENST00000592643.1:c.63G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000468714
  ensembl transcript: ENST00000587560
  gene symbol: H3F3B
  hgvsc: ENST00000587560.1:c.63G>A
  hgvsp: ENST00000587560.1:c.63G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000466663
  ensembl transcript: ENST00000591890
  gene symbol: H3F3B
  hgvsc: ENST00000591890.1:c.63G>A
  hgvsp: ENST00000591890.1:c.63G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000586518
  gene symbol: H3F3B
  hgvsc: ENST00000586518.1:n.661G>A
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000589949
  gene symbol: H3F3B
  hgvsc: ENST00000589949.1:n.183G>A
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000466020
  ensembl transcript: ENST00000586607
  gene symbol: H3F3B
  hgvsc: ENST00000586607.1:c.63G>A
  hgvsp: ENST00000586607.1:c.63G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000468484
  ensembl transcript: ENST00000587171
  gene symbol: H3F3B
  hgvsc: ENST00000587171.1:c.63G>A
  hgvsp: ENST00000587171.1:c.63G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4765
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1197
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2578
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25535
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 554
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22327
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2638
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5292
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu21Leu
num of homozygotes: 0
population: Other
population: South Asian
population: African
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
reference allele: C
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum

17-73775195-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73775195
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 73775195
    reference: chr 17
allele count: 5
allele frequency: 4.328704505315649e-5
allele num: 115508
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000254810
  ensembl transcript: ENST00000254810
  gene symbol: H3F3B
  hgvsc: ENST00000254810.4:c.61C>T
  hgvsp: ENST00000254810.4:c.61C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000466663
  ensembl transcript: ENST00000591890
  gene symbol: H3F3B
  hgvsc: ENST00000591890.1:c.61C>T
  hgvsp: ENST00000591890.1:c.61C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000466020
  ensembl transcript: ENST00000586607
  gene symbol: H3F3B
  hgvsc: ENST00000586607.1:c.61C>T
  hgvsp: ENST00000586607.1:c.61C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000593254
  gene symbol: H3F3B
  hgvsc: ENST00000593254.1:n.118-232C>T
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000589949
  gene symbol: H3F3B
  hgvsc: ENST00000589949.1:n.181C>T
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000468484
  ensembl transcript: ENST00000587171
  gene symbol: H3F3B
  hgvsc: ENST00000587171.1:c.61C>T
  hgvsp: ENST00000587171.1:c.61C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000465403
  ensembl transcript: ENST00000586270
  gene symbol: H3F3B
  hgvsc: ENST00000586270.1:c.61C>T
  hgvsp: ENST00000586270.1:c.61C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000586518
  gene symbol: H3F3B
  hgvsc: ENST00000586518.1:n.659C>T
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000465813
  ensembl transcript: ENST00000589599
  gene symbol: H3F3B
  hgvsc: ENST00000589599.1:c.61C>T
  hgvsp: ENST00000589599.1:c.61C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000468714
  ensembl transcript: ENST00000587560
  gene symbol: H3F3B
  hgvsc: ENST00000587560.1:c.61C>T
  hgvsp: ENST00000587560.1:c.61C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000467165
  ensembl transcript: ENST00000592643
  gene symbol: H3F3B
  hgvsc: ENST00000592643.1:c.61C>T
  hgvsp: ENST00000592643.1:c.61C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000589417
  gene symbol: H3F3B
  hgvsc: ENST00000589417.1:n.194C>T
  variant of: http://identifiers.org/hgnc/4765
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 560
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2540
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25560
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 22367
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2657
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1131
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5294
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu21Leu
num of homozygotes: 0
population: South Asian
population: Latino
population: African
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
reference allele: G
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: DP

17-73775203-C-CG
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73775203
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 73775204
    reference: chr 17
allele count: 1
allele frequency: 8.696862172128297e-6
allele num: 114984
alternate allele: CG
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000589417
  gene symbol: H3F3B
  hgvsc: ENST00000589417.1:n.185dupC
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000466663
  ensembl transcript: ENST00000591890
  gene symbol: H3F3B
  hgvsc: ENST00000591890.1:c.52dupC
  hgvsp: ENSP00000466663.1:p.Arg18ProfsTer118
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000466020
  ensembl transcript: ENST00000586607
  gene symbol: H3F3B
  hgvsc: ENST00000586607.1:c.52dupC
  hgvsp: ENSP00000466020.1:p.Arg18ProfsTer80
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000468484
  ensembl transcript: ENST00000587171
  gene symbol: H3F3B
  hgvsc: ENST00000587171.1:c.52dupC
  hgvsp: ENSP00000468484.1:p.Arg18ProfsTer98
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000468714
  ensembl transcript: ENST00000587560
  gene symbol: H3F3B
  hgvsc: ENST00000587560.1:c.52dupC
  hgvsp: ENSP00000468714.1:p.Arg18ProfsTer80
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000465813
  ensembl transcript: ENST00000589599
  gene symbol: H3F3B
  hgvsc: ENST00000589599.1:c.52dupC
  hgvsp: ENSP00000465813.1:p.Arg18ProfsTer80
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000254810
  ensembl transcript: ENST00000254810
  gene symbol: H3F3B
  hgvsc: ENST00000254810.4:c.52dupC
  hgvsp: ENSP00000254810.3:p.Arg18ProfsTer80
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000586518
  gene symbol: H3F3B
  hgvsc: ENST00000586518.1:n.650dupC
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000467165
  ensembl transcript: ENST00000592643
  gene symbol: H3F3B
  hgvsc: ENST00000592643.1:c.52dupC
  hgvsp: ENSP00000467165.1:p.Arg18ProfsTer96
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000593254
  gene symbol: H3F3B
  hgvsc: ENST00000593254.1:n.118-241dupC
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000465403
  ensembl transcript: ENST00000586270
  gene symbol: H3F3B
  hgvsc: ENST00000586270.1:c.52dupC
  hgvsp: ENSP00000465403.1:p.Arg18ProfsTer80
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000589949
  gene symbol: H3F3B
  hgvsc: ENST00000589949.1:n.172dupC
  variant of: http://identifiers.org/hgnc/4765
canonical: true
consequence: frameshift
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25608
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2516
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22396
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5363
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 870
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2753
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg18ProfsTer80
num of homozygotes: 0
population: African
population: East Asian
population: South Asian
population: Other
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
reference allele: C
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum

17-73775205-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73775205
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 73775205
    reference: chr 17
allele count: 2
allele frequency: 1.737740242588538e-5
allele num: 115092
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000465403
  ensembl transcript: ENST00000586270
  gene symbol: H3F3B
  hgvsc: ENST00000586270.1:c.51C>T
  hgvsp: ENST00000586270.1:c.51C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000466020
  ensembl transcript: ENST00000586607
  gene symbol: H3F3B
  hgvsc: ENST00000586607.1:c.51C>T
  hgvsp: ENST00000586607.1:c.51C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000589949
  gene symbol: H3F3B
  hgvsc: ENST00000589949.1:n.171C>T
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000586518
  gene symbol: H3F3B
  hgvsc: ENST00000586518.1:n.649C>T
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000466663
  ensembl transcript: ENST00000591890
  gene symbol: H3F3B
  hgvsc: ENST00000591890.1:c.51C>T
  hgvsp: ENST00000591890.1:c.51C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000468714
  ensembl transcript: ENST00000587560
  gene symbol: H3F3B
  hgvsc: ENST00000587560.1:c.51C>T
  hgvsp: ENST00000587560.1:c.51C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000465813
  ensembl transcript: ENST00000589599
  gene symbol: H3F3B
  hgvsc: ENST00000589599.1:c.51C>T
  hgvsp: ENST00000589599.1:c.51C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000589417
  gene symbol: H3F3B
  hgvsc: ENST00000589417.1:n.184C>T
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000468484
  ensembl transcript: ENST00000587171
  gene symbol: H3F3B
  hgvsc: ENST00000587171.1:c.51C>T
  hgvsp: ENST00000587171.1:c.51C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000254810
  ensembl transcript: ENST00000254810
  gene symbol: H3F3B
  hgvsc: ENST00000254810.4:c.51C>T
  hgvsp: ENST00000254810.4:c.51C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000467165
  ensembl transcript: ENST00000592643
  gene symbol: H3F3B
  hgvsc: ENST00000592643.1:c.51C>T
  hgvsp: ENST00000592643.1:c.51C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000593254
  gene symbol: H3F3B
  hgvsc: ENST00000593254.1:n.118-242C>T
  variant of: http://identifiers.org/hgnc/4765
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22465
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5308
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 735
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2501
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2831
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25669
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro17Pro
num of homozygotes: 0
population: South Asian
population: Latino
population: African
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
reference allele: G
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: BaseQRankSum

17-73775205-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73775205
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 73775205
    reference: chr 17
allele count: 5
allele frequency: 4.344350606471345e-5
allele num: 115092
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000467165
  ensembl transcript: ENST00000592643
  gene symbol: H3F3B
  hgvsc: ENST00000592643.1:c.51C>G
  hgvsp: ENST00000592643.1:c.51C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000466663
  ensembl transcript: ENST00000591890
  gene symbol: H3F3B
  hgvsc: ENST00000591890.1:c.51C>G
  hgvsp: ENST00000591890.1:c.51C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000465403
  ensembl transcript: ENST00000586270
  gene symbol: H3F3B
  hgvsc: ENST00000586270.1:c.51C>G
  hgvsp: ENST00000586270.1:c.51C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000468484
  ensembl transcript: ENST00000587171
  gene symbol: H3F3B
  hgvsc: ENST00000587171.1:c.51C>G
  hgvsp: ENST00000587171.1:c.51C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000589949
  gene symbol: H3F3B
  hgvsc: ENST00000589949.1:n.171C>G
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000468714
  ensembl transcript: ENST00000587560
  gene symbol: H3F3B
  hgvsc: ENST00000587560.1:c.51C>G
  hgvsp: ENST00000587560.1:c.51C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000586518
  gene symbol: H3F3B
  hgvsc: ENST00000586518.1:n.649C>G
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000465813
  ensembl transcript: ENST00000589599
  gene symbol: H3F3B
  hgvsc: ENST00000589599.1:c.51C>G
  hgvsp: ENST00000589599.1:c.51C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000593254
  gene symbol: H3F3B
  hgvsc: ENST00000593254.1:n.118-242C>G
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000466020
  ensembl transcript: ENST00000586607
  gene symbol: H3F3B
  hgvsc: ENST00000586607.1:c.51C>G
  hgvsp: ENST00000586607.1:c.51C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000589417
  gene symbol: H3F3B
  hgvsc: ENST00000589417.1:n.184C>G
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000254810
  ensembl transcript: ENST00000254810
  gene symbol: H3F3B
  hgvsc: ENST00000254810.4:c.51C>G
  hgvsp: ENST00000254810.4:c.51C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/4765
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25669
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22465
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 565
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 735
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2501
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2831
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5308
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 4.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Pro17Pro
num of homozygotes: 0
population: Other
population: European (Finnish)
population: South Asian
population: East Asian
population: African
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum

17-73775205-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73775205
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 73775205
    reference: chr 17
allele count: 2
allele frequency: 1.737740242588538e-5
allele num: 115092
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000466020
  ensembl transcript: ENST00000586607
  gene symbol: H3F3B
  hgvsc: ENST00000586607.1:c.51C>A
  hgvsp: ENST00000586607.1:c.51C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000254810
  ensembl transcript: ENST00000254810
  gene symbol: H3F3B
  hgvsc: ENST00000254810.4:c.51C>A
  hgvsp: ENST00000254810.4:c.51C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000589417
  gene symbol: H3F3B
  hgvsc: ENST00000589417.1:n.184C>A
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000465403
  ensembl transcript: ENST00000586270
  gene symbol: H3F3B
  hgvsc: ENST00000586270.1:c.51C>A
  hgvsp: ENST00000586270.1:c.51C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000465813
  ensembl transcript: ENST00000589599
  gene symbol: H3F3B
  hgvsc: ENST00000589599.1:c.51C>A
  hgvsp: ENST00000589599.1:c.51C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000589949
  gene symbol: H3F3B
  hgvsc: ENST00000589949.1:n.171C>A
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000466663
  ensembl transcript: ENST00000591890
  gene symbol: H3F3B
  hgvsc: ENST00000591890.1:c.51C>A
  hgvsp: ENST00000591890.1:c.51C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000467165
  ensembl transcript: ENST00000592643
  gene symbol: H3F3B
  hgvsc: ENST00000592643.1:c.51C>A
  hgvsp: ENST00000592643.1:c.51C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000593254
  gene symbol: H3F3B
  hgvsc: ENST00000593254.1:n.118-242C>A
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000586518
  gene symbol: H3F3B
  hgvsc: ENST00000586518.1:n.649C>A
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000468714
  ensembl transcript: ENST00000587560
  gene symbol: H3F3B
  hgvsc: ENST00000587560.1:c.51C>A
  hgvsp: ENST00000587560.1:c.51C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000468484
  ensembl transcript: ENST00000587171
  gene symbol: H3F3B
  hgvsc: ENST00000587171.1:c.51C>A
  hgvsp: ENST00000587171.1:c.51C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4765
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 22465
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25669
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 735
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2501
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2831
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5308
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro17Pro
num of homozygotes: 0
population: African
population: European (Finnish)
population: South Asian
population: East Asian
population: Latino
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: MQ

17-73775208-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73775208
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 73775208
    reference: chr 17
allele count: 6
allele frequency: 5.221295925648746e-5
allele num: 114914
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000468484
  ensembl transcript: ENST00000587171
  gene symbol: H3F3B
  hgvsc: ENST00000587171.1:c.48C>T
  hgvsp: ENST00000587171.1:c.48C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000465813
  ensembl transcript: ENST00000589599
  gene symbol: H3F3B
  hgvsc: ENST00000589599.1:c.48C>T
  hgvsp: ENST00000589599.1:c.48C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000467165
  ensembl transcript: ENST00000592643
  gene symbol: H3F3B
  hgvsc: ENST00000592643.1:c.48C>T
  hgvsp: ENST00000592643.1:c.48C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000593254
  gene symbol: H3F3B
  hgvsc: ENST00000593254.1:n.118-245C>T
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000468714
  ensembl transcript: ENST00000587560
  gene symbol: H3F3B
  hgvsc: ENST00000587560.1:c.48C>T
  hgvsp: ENST00000587560.1:c.48C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000586518
  gene symbol: H3F3B
  hgvsc: ENST00000586518.1:n.646C>T
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000465403
  ensembl transcript: ENST00000586270
  gene symbol: H3F3B
  hgvsc: ENST00000586270.1:c.48C>T
  hgvsp: ENST00000586270.1:c.48C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000589949
  gene symbol: H3F3B
  hgvsc: ENST00000589949.1:n.168C>T
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000254810
  ensembl transcript: ENST00000254810
  gene symbol: H3F3B
  hgvsc: ENST00000254810.4:c.48C>T
  hgvsp: ENST00000254810.4:c.48C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000466663
  ensembl transcript: ENST00000591890
  gene symbol: H3F3B
  hgvsc: ENST00000591890.1:c.48C>T
  hgvsp: ENST00000591890.1:c.48C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000589417
  gene symbol: H3F3B
  hgvsc: ENST00000589417.1:n.181C>T
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000466020
  ensembl transcript: ENST00000586607
  gene symbol: H3F3B
  hgvsc: ENST00000586607.1:c.48C>T
  hgvsp: ENST00000586607.1:c.48C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4765
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25665
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22356
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2934
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 690
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5295
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2576
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 559
  bin: 3.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Ala16Ala
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: Other
population: Latino
population: European (Finnish)
population: East Asian
population: African
reference allele: G
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff

17-73775208-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73775208
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 73775208
    reference: chr 17
allele count: 2
allele frequency: 1.740431975216249e-5
allele num: 114914
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000468714
  ensembl transcript: ENST00000587560
  gene symbol: H3F3B
  hgvsc: ENST00000587560.1:c.48C>A
  hgvsp: ENST00000587560.1:c.48C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000589949
  gene symbol: H3F3B
  hgvsc: ENST00000589949.1:n.168C>A
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000586518
  gene symbol: H3F3B
  hgvsc: ENST00000586518.1:n.646C>A
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000466020
  ensembl transcript: ENST00000586607
  gene symbol: H3F3B
  hgvsc: ENST00000586607.1:c.48C>A
  hgvsp: ENST00000586607.1:c.48C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000467165
  ensembl transcript: ENST00000592643
  gene symbol: H3F3B
  hgvsc: ENST00000592643.1:c.48C>A
  hgvsp: ENST00000592643.1:c.48C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000465403
  ensembl transcript: ENST00000586270
  gene symbol: H3F3B
  hgvsc: ENST00000586270.1:c.48C>A
  hgvsp: ENST00000586270.1:c.48C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000254810
  ensembl transcript: ENST00000254810
  gene symbol: H3F3B
  hgvsc: ENST00000254810.4:c.48C>A
  hgvsp: ENST00000254810.4:c.48C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000468484
  ensembl transcript: ENST00000587171
  gene symbol: H3F3B
  hgvsc: ENST00000587171.1:c.48C>A
  hgvsp: ENST00000587171.1:c.48C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000466663
  ensembl transcript: ENST00000591890
  gene symbol: H3F3B
  hgvsc: ENST00000591890.1:c.48C>A
  hgvsp: ENST00000591890.1:c.48C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000589417
  gene symbol: H3F3B
  hgvsc: ENST00000589417.1:n.181C>A
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000593254
  gene symbol: H3F3B
  hgvsc: ENST00000593254.1:n.118-245C>A
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000465813
  ensembl transcript: ENST00000589599
  gene symbol: H3F3B
  hgvsc: ENST00000589599.1:c.48C>A
  hgvsp: ENST00000589599.1:c.48C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4765
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 559
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2576
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22356
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 25665
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 690
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2934
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala16Ala
num of homozygotes: 0
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: East Asian
population: Latino
population: South Asian
reference allele: G
site quality: MQ
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum

17-73775217-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73775217
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 73775217
    reference: chr 17
allele count: 2
allele frequency: 1.75324789171941e-5
allele num: 114074
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000465403
  ensembl transcript: ENST00000586270
  gene symbol: H3F3B
  hgvsc: ENST00000586270.1:c.39T>C
  hgvsp: ENST00000586270.1:c.39T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000586518
  gene symbol: H3F3B
  hgvsc: ENST00000586518.1:n.637T>C
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000589949
  gene symbol: H3F3B
  hgvsc: ENST00000589949.1:n.159T>C
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000468484
  ensembl transcript: ENST00000587171
  gene symbol: H3F3B
  hgvsc: ENST00000587171.1:c.39T>C
  hgvsp: ENST00000587171.1:c.39T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000466020
  ensembl transcript: ENST00000586607
  gene symbol: H3F3B
  hgvsc: ENST00000586607.1:c.39T>C
  hgvsp: ENST00000586607.1:c.39T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000465813
  ensembl transcript: ENST00000589599
  gene symbol: H3F3B
  hgvsc: ENST00000589599.1:c.39T>C
  hgvsp: ENST00000589599.1:c.39T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000593254
  gene symbol: H3F3B
  hgvsc: ENST00000593254.1:n.118-254T>C
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000466663
  ensembl transcript: ENST00000591890
  gene symbol: H3F3B
  hgvsc: ENST00000591890.1:c.39T>C
  hgvsp: ENST00000591890.1:c.39T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000468714
  ensembl transcript: ENST00000587560
  gene symbol: H3F3B
  hgvsc: ENST00000587560.1:c.39T>C
  hgvsp: ENST00000587560.1:c.39T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000467165
  ensembl transcript: ENST00000592643
  gene symbol: H3F3B
  hgvsc: ENST00000592643.1:c.39T>C
  hgvsp: ENST00000592643.1:c.39T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000254810
  ensembl transcript: ENST00000254810
  gene symbol: H3F3B
  hgvsc: ENST00000254810.4:c.39T>C
  hgvsp: ENST00000254810.4:c.39T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000589417
  gene symbol: H3F3B
  hgvsc: ENST00000589417.1:n.172T>C
  variant of: http://identifiers.org/hgnc/4765
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3255
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 335
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 603
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2870
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5289
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25642
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 553
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly13Gly
num of homozygotes: 0
population: Other
population: Latino
population: African
population: European (Finnish)
population: East Asian
population: South Asian
population: European (Non-Finnish)
reference allele: A
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: QD

17-73775217-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73775217
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 73775217
    reference: chr 17
allele count: 1
allele frequency: 8.76623945859705e-6
allele num: 114074
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000465813
  ensembl transcript: ENST00000589599
  gene symbol: H3F3B
  hgvsc: ENST00000589599.1:c.39T>A
  hgvsp: ENST00000589599.1:c.39T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000589417
  gene symbol: H3F3B
  hgvsc: ENST00000589417.1:n.172T>A
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000586518
  gene symbol: H3F3B
  hgvsc: ENST00000586518.1:n.637T>A
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000466663
  ensembl transcript: ENST00000591890
  gene symbol: H3F3B
  hgvsc: ENST00000591890.1:c.39T>A
  hgvsp: ENST00000591890.1:c.39T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000468714
  ensembl transcript: ENST00000587560
  gene symbol: H3F3B
  hgvsc: ENST00000587560.1:c.39T>A
  hgvsp: ENST00000587560.1:c.39T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000593254
  gene symbol: H3F3B
  hgvsc: ENST00000593254.1:n.118-254T>A
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000465403
  ensembl transcript: ENST00000586270
  gene symbol: H3F3B
  hgvsc: ENST00000586270.1:c.39T>A
  hgvsp: ENST00000586270.1:c.39T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000467165
  ensembl transcript: ENST00000592643
  gene symbol: H3F3B
  hgvsc: ENST00000592643.1:c.39T>A
  hgvsp: ENST00000592643.1:c.39T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000468484
  ensembl transcript: ENST00000587171
  gene symbol: H3F3B
  hgvsc: ENST00000587171.1:c.39T>A
  hgvsp: ENST00000587171.1:c.39T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000254810
  ensembl transcript: ENST00000254810
  gene symbol: H3F3B
  hgvsc: ENST00000254810.4:c.39T>A
  hgvsp: ENST00000254810.4:c.39T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000466020
  ensembl transcript: ENST00000586607
  gene symbol: H3F3B
  hgvsc: ENST00000586607.1:c.39T>A
  hgvsp: ENST00000586607.1:c.39T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000589949
  gene symbol: H3F3B
  hgvsc: ENST00000589949.1:n.159T>A
  variant of: http://identifiers.org/hgnc/4765
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25642
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21796
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2870
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 335
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 553
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5289
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 603
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3255
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly13Gly
num of homozygotes: 0
population: African
population: South Asian
population: Latino
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: A
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: QD

17-73775220-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73775220
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 73775220
    reference: chr 17
allele count: 1
allele frequency: 8.79600309619309e-6
allele num: 113688
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000586518
  gene symbol: H3F3B
  hgvsc: ENST00000586518.1:n.634C>G
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000465403
  ensembl transcript: ENST00000586270
  gene symbol: H3F3B
  hgvsc: ENST00000586270.1:c.36C>G
  hgvsp: ENST00000586270.1:c.36C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000468484
  ensembl transcript: ENST00000587171
  gene symbol: H3F3B
  hgvsc: ENST00000587171.1:c.36C>G
  hgvsp: ENST00000587171.1:c.36C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000466663
  ensembl transcript: ENST00000591890
  gene symbol: H3F3B
  hgvsc: ENST00000591890.1:c.36C>G
  hgvsp: ENST00000591890.1:c.36C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000589417
  gene symbol: H3F3B
  hgvsc: ENST00000589417.1:n.169C>G
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000467165
  ensembl transcript: ENST00000592643
  gene symbol: H3F3B
  hgvsc: ENST00000592643.1:c.36C>G
  hgvsp: ENST00000592643.1:c.36C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000468714
  ensembl transcript: ENST00000587560
  gene symbol: H3F3B
  hgvsc: ENST00000587560.1:c.36C>G
  hgvsp: ENST00000587560.1:c.36C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000254810
  ensembl transcript: ENST00000254810
  gene symbol: H3F3B
  hgvsc: ENST00000254810.4:c.36C>G
  hgvsp: ENST00000254810.4:c.36C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000465813
  ensembl transcript: ENST00000589599
  gene symbol: H3F3B
  hgvsc: ENST00000589599.1:c.36C>G
  hgvsp: ENST00000589599.1:c.36C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000466020
  ensembl transcript: ENST00000586607
  gene symbol: H3F3B
  hgvsc: ENST00000586607.1:c.36C>G
  hgvsp: ENST00000586607.1:c.36C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000589949
  gene symbol: H3F3B
  hgvsc: ENST00000589949.1:n.156C>G
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000593254
  gene symbol: H3F3B
  hgvsc: ENST00000593254.1:n.118-257C>G
  variant of: http://identifiers.org/hgnc/4765
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21535
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 379
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3394
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 557
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25609
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5301
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3006
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr12Thr
num of homozygotes: 0
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: Latino
population: South Asian
population: African
population: East Asian
reference allele: G
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD

17-73775232-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73775232
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 73775232
    reference: chr 17
allele count: 1
allele frequency: 8.923472301541976e-6
allele num: 112064
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000465403
  ensembl transcript: ENST00000586270
  gene symbol: H3F3B
  hgvsc: ENST00000586270.1:c.24T>A
  hgvsp: ENST00000586270.1:c.24T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000254810
  ensembl transcript: ENST00000254810
  gene symbol: H3F3B
  hgvsc: ENST00000254810.4:c.24T>A
  hgvsp: ENST00000254810.4:c.24T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000466020
  ensembl transcript: ENST00000586607
  gene symbol: H3F3B
  hgvsc: ENST00000586607.1:c.24T>A
  hgvsp: ENST00000586607.1:c.24T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000589417
  gene symbol: H3F3B
  hgvsc: ENST00000589417.1:n.157T>A
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000468484
  ensembl transcript: ENST00000587171
  gene symbol: H3F3B
  hgvsc: ENST00000587171.1:c.24T>A
  hgvsp: ENST00000587171.1:c.24T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000468714
  ensembl transcript: ENST00000587560
  gene symbol: H3F3B
  hgvsc: ENST00000587560.1:c.24T>A
  hgvsp: ENST00000587560.1:c.24T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000466663
  ensembl transcript: ENST00000591890
  gene symbol: H3F3B
  hgvsc: ENST00000591890.1:c.24T>A
  hgvsp: ENST00000591890.1:c.24T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000465813
  ensembl transcript: ENST00000589599
  gene symbol: H3F3B
  hgvsc: ENST00000589599.1:c.24T>A
  hgvsp: ENST00000589599.1:c.24T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000593254
  gene symbol: H3F3B
  hgvsc: ENST00000593254.1:n.118-269T>A
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000586518
  gene symbol: H3F3B
  hgvsc: ENST00000586518.1:n.622T>A
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132475
  ensembl protein: ENSP00000467165
  ensembl transcript: ENST00000592643
  gene symbol: H3F3B
  hgvsc: ENST00000592643.1:c.24T>A
  hgvsp: ENST00000592643.1:c.24T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4765
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000132475
  ensembl transcript: ENST00000589949
  gene symbol: H3F3B
  hgvsc: ENST00000589949.1:n.144T>A
  variant of: http://identifiers.org/hgnc/4765
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3585
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20489
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25354
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5217
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 654
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 541
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3957
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 544
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala8Ala
num of homozygotes: 0
reference allele: A

GenotypeDepth
all individuals: 106
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 9
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 36
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 41
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10495
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 903
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 13
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 194
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 85
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 67
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3019
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 687
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 59
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2792
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 175
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1202
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 136
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 401
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 39958
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 414
bin: 9.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8634
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.512172992590352e-5
allele num: 66130
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6606
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11548
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16510
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10316
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.675487e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.2e-3

FS
type: SiteQuality
SIO_000300: 8.6e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.36e-1

MQ
type: SiteQuality
SIO_000300: 4.996e1

VQSLOD
type: SiteQuality
SIO_000300: -1.9e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.74e0

MQRankSum
type: SiteQuality
SIO_000300: 1.27e0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.36e-1

QD
type: SiteQuality
SIO_000300: 1.149e1

GenotypeDepth
all individuals: 11510
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 106
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 30
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 103
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 194
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 39632
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 824
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2992
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 106
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 69
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 61
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 234
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 97
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 257
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 890
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 18
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 10410
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 394
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1186
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 409
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2760
bin: 7.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8626
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10272
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16508
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6600
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.668515950069348e-5
allele num: 11536
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66000
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.351e0

DP
type: SiteQuality
SIO_000300: 1.668931e6

MQRankSum
type: SiteQuality
SIO_000300: -4.29e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.54e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.718e0

FS
type: SiteQuality
SIO_000300: 8.39e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.407e1

QD
type: SiteQuality
SIO_000300: 1.144e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.202e0

GenotypeDepth
all individuals: 36
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2275
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 12688
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 9
bin: 9.25e1
variant carriers: 1

GenotypeQuality
all individuals: 103
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 10302
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2683
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 384
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 46
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 54
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 215
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 136
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 280
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 271
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 148
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 377
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 146
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 848
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1141
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2942
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1008
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 115
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 39491
bin: 6.25e1
variant carriers: 0

Other
type: Population
allele count: 1
allele frequency: 1.106194690265487e-3
allele num: 904
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10218
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11522
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
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East Asian
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allele frequency: 0.0e0
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num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 0.0e0
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num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.662737e6

MQ
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SIO_000300: 5.693e1

ClippingRankSum
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SIO_000300: 3.72e0

FS
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QD
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InbreedingCoeff
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ReadPosRankSum
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MQRankSum
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SIO_000300: -3.4e-1

BaseQRankSum
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SIO_000300: 3.4e-1

VQSLOD
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SIO_000300: -2.995e0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 1.25e1
variant carriers: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11506
num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
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num of homozygotes: 0

African
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allele frequency: 0.0e0
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num of homozygotes: 0

South Asian
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Other
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 0.0e0
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East Asian
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ReadPosRankSum
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SIO_000300: -1.113e0

InbreedingCoeff
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MQ
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BaseQRankSum
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MQRankSum
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DP
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VQSLOD
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FS
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SIO_000300: 8.342000000000001e0

QD
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SIO_000300: 1.294e1

ClippingRankSum
type: SiteQuality
SIO_000300: 9.72e-1

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 2

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

South Asian
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allele frequency: 1.21197430614471e-4
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European (Non-Finnish)
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allele frequency: 0.0e0
allele num: 65758
num of homozygotes: 0

African
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
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InbreedingCoeff
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SIO_000300: 4.2e-3

FS
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SIO_000300: 5.47e-1

BaseQRankSum
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VQSLOD
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ReadPosRankSum
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ClippingRankSum
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MQ
type: SiteQuality
SIO_000300: 5.366e1

QD
type: SiteQuality
SIO_000300: 1.087e1

DP
type: SiteQuality
SIO_000300: 1.651563e6

MQRankSum
type: SiteQuality
SIO_000300: 2.68e-1

GenotypeDepth
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variant carriers: 2

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 15

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 3.25e1
variant carriers: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16494
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.524855138761818e-4
allele num: 6558
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 900
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Latino
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allele frequency: 1.738223535546671e-4
allele num: 11506
num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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allele count: 12
allele frequency: 1.825206096188361e-4
allele num: 65746
num of homozygotes: 0

African
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num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.2e0

QD
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InbreedingCoeff
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MQRankSum
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MQ
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ReadPosRankSum
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DP
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SIO_000300: 1.650588e6

VQSLOD
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SIO_000300: -9.751e-1

BaseQRankSum
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SIO_000300: -2.76e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.51e-1

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6556
num of homozygotes: 0

East Asian
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allele frequency: 2.325040688212044e-4
allele num: 8602
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South Asian
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allele frequency: 0.0e0
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African
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Other
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Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11504
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European (Non-Finnish)
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VQSLOD
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MQ
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FS
type: SiteQuality
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InbreedingCoeff
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DP
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BaseQRankSum
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MQRankSum
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ReadPosRankSum
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QD
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ClippingRankSum
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GenotypeDepth
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variant carriers: 2

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 143

Other
type: Population
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allele num: 902
num of homozygotes: 0

Latino
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allele frequency: 6.08695652173913e-4
allele num: 11500
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South Asian
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East Asian
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allele frequency: 1.163061177017911e-4
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African
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allele frequency: 1.32534851757314e-2
allele num: 10186
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European (Non-Finnish)
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allele frequency: 3.044788843893676e-5
allele num: 65686
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European (Finnish)
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MQRankSum
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VQSLOD
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InbreedingCoeff
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QD
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ReadPosRankSum
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ClippingRankSum
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MQ
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FS
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BaseQRankSum
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DP
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

East Asian
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European (Finnish)
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African
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Latino
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South Asian
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Other
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European (Non-Finnish)
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ReadPosRankSum
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DP
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VQSLOD
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QD
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BaseQRankSum
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MQRankSum
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FS
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ClippingRankSum
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InbreedingCoeff
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MQ
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6550
num of homozygotes: 0

African
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allele frequency: 9.813542688910697e-5
allele num: 10190
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European (Non-Finnish)
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East Asian
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South Asian
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Latino
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Other
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FS
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MQRankSum
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VQSLOD
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ReadPosRankSum
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SIO_000300: -5.590000000000001e-1

InbreedingCoeff
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DP
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BaseQRankSum
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SIO_000300: -2.52e0

ClippingRankSum
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SIO_000300: 4.93e-1

MQ
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SIO_000300: 5.554e1

QD
type: SiteQuality
SIO_000300: 1.525e1

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 8.25e1
variant carriers: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8598
num of homozygotes: 0

African
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allele frequency: 0.0e0
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num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
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num of homozygotes: 0

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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allele count: 3
allele frequency: 4.570383912248629e-5
allele num: 65640
num of homozygotes: 0

South Asian
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FS
type: SiteQuality
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InbreedingCoeff
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MQ
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ReadPosRankSum
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VQSLOD
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BaseQRankSum
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MQRankSum
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ClippingRankSum
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DP
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QD
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 6

European (Finnish)
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allele frequency: 0.0e0
allele num: 6544
num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 6.092916984006093e-5
allele num: 65650
num of homozygotes: 0

South Asian
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allele num: 16492
num of homozygotes: 0

Latino
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allele frequency: 8.698677800974252e-5
allele num: 11496
num of homozygotes: 0

African
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allele frequency: 0.0e0
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Other
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BaseQRankSum
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SIO_000300: -2.514e0

ClippingRankSum
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ReadPosRankSum
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MQRankSum
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FS
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VQSLOD
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InbreedingCoeff
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MQ
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QD
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DP
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SIO_000300: 1.640117e6

GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6538
num of homozygotes: 0

Other
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 2
allele frequency: 3.050919852335479e-5
allele num: 65554
num of homozygotes: 0

African
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allele frequency: 0.0e0
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Latino
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allele num: 11480
num of homozygotes: 0

East Asian
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South Asian
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FS
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SIO_000300: 4.41e0

ReadPosRankSum
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ClippingRankSum
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BaseQRankSum
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MQRankSum
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QD
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MQ
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DP
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VQSLOD
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InbreedingCoeff
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SIO_000300: 3.0e-3

GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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allele frequency: 6.071645415907711e-5
allele num: 16470
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
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African
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 0.0e0
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East Asian
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Other
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ReadPosRankSum
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InbreedingCoeff
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BaseQRankSum
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FS
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QD
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MQRankSum
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VQSLOD
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ClippingRankSum
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DP
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MQ
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GenotypeDepth
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 65418
num of homozygotes: 0

Latino
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allele num: 11464
num of homozygotes: 0

African
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South Asian
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East Asian
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Other
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European (Finnish)
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FS
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ReadPosRankSum
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VQSLOD
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MQRankSum
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BaseQRankSum
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DP
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QD
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InbreedingCoeff
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ClippingRankSum
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MQ
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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num of homozygotes: 0

East Asian
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European (Finnish)
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Other
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European (Non-Finnish)
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Latino
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South Asian
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InbreedingCoeff
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QD
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ClippingRankSum
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MQRankSum
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FS
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MQ
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BaseQRankSum
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VQSLOD
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DP
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ReadPosRankSum
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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allele num: 10080
num of homozygotes: 0

Other
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East Asian
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South Asian
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Latino
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European (Finnish)
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European (Non-Finnish)
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ClippingRankSum
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DP
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BaseQRankSum
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MQRankSum
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QD
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InbreedingCoeff
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VQSLOD
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FS
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ReadPosRankSum
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MQ
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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allele frequency: 0.0e0
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num of homozygotes: 0

African
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allele frequency: 0.0e0
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Other
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South Asian
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East Asian
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European (Non-Finnish)
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allele frequency: 0.0e0
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num of homozygotes: 0

Latino
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num of homozygotes: 0

InbreedingCoeff
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QD
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MQRankSum
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ReadPosRankSum
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MQ
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ClippingRankSum
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DP
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VQSLOD
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BaseQRankSum
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FS
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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allele frequency: 1.052385406922357e-3
allele num: 8552
num of homozygotes: 0

African
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Other
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Latino
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South Asian
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European (Non-Finnish)
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allele num: 65160
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European (Finnish)
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ClippingRankSum
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MQ
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DP
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ReadPosRankSum
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MQRankSum
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FS
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QD
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InbreedingCoeff
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VQSLOD
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BaseQRankSum
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

East Asian
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num of homozygotes: 0

African
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European (Finnish)
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European (Non-Finnish)
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Latino
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allele num: 11426
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Other
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South Asian
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QD
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MQ
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FS
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ClippingRankSum
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DP
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VQSLOD
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ReadPosRankSum
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InbreedingCoeff
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MQRankSum
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BaseQRankSum
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GenotypeDepth
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 64642
num of homozygotes: 0

African
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allele num: 10000
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East Asian
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European (Finnish)
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South Asian
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Other
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Latino
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ReadPosRankSum
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InbreedingCoeff
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BaseQRankSum
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VQSLOD
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ClippingRankSum
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MQ
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FS
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MQRankSum
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DP
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QD
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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num of homozygotes: 0

European (Non-Finnish)
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Latino
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allele num: 11384
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African
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South Asian
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European (Finnish)
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East Asian
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ClippingRankSum
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InbreedingCoeff
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QD
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BaseQRankSum
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FS
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VQSLOD
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MQRankSum
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DP
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MQ
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ReadPosRankSum
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GenotypeDepth
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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num of homozygotes: 0

Other
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Latino
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num of homozygotes: 0

European (Non-Finnish)
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African
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East Asian
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European (Finnish)
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MQRankSum
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MQ
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BaseQRankSum
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QD
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ClippingRankSum
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FS
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VQSLOD
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InbreedingCoeff
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ReadPosRankSum
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DP
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GenotypeDepth
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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Other
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European (Finnish)
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South Asian
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Latino
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European (Non-Finnish)
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African
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InbreedingCoeff
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MQRankSum
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BaseQRankSum
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QD
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DP
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ReadPosRankSum
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VQSLOD
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FS
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MQ
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ClippingRankSum
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GenotypeDepth
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 448
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2006
bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 258
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 840
bin: 4.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6360
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16202
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 870
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.561134007743225e-5
allele num: 64056
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9886
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8498
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11326
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.61e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.582e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.5e-3

QD
type: SiteQuality
SIO_000300: 1.415e1

DP
type: SiteQuality
SIO_000300: 1.481963e6

BaseQRankSum
type: SiteQuality
SIO_000300: -4.2e-1

VQSLOD
type: SiteQuality
SIO_000300: 7.38e-1

FS
type: SiteQuality
SIO_000300: 3.151e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.182e0

MQ
type: SiteQuality
SIO_000300: 5.335e1

GenotypeQuality
all individuals: 644
bin: 9.75e1
variant carriers: 2

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6762
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 306
bin: 9.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11328
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16178
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8488
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.121975586150917e-5
allele num: 64062
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6398
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9908
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 872
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.478057e6

MQRankSum
type: SiteQuality
SIO_000300: -2.781e0

FS
type: SiteQuality
SIO_000300: 2.495e0

QD
type: SiteQuality
SIO_000300: 3.74e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.158e0

VQSLOD
type: SiteQuality
SIO_000300: 3.86e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.08e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.2e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -4.42e-1

MQ
type: SiteQuality
SIO_000300: 5.115e1

GenotypeDepth
all individuals: 55
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 164
bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6652
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variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1711
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variant carriers: 0

GenotypeQuality
all individuals: 403
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variant carriers: 0

GenotypeQuality
all individuals: 1916
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GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 274
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 634
bin: 9.75e1
variant carriers: 3

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6390
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8478
num of homozygotes: 0

Latino
type: Population
allele count: 3
allele frequency: 2.648772735299311e-4
allele num: 11326
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16136
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9908
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63974
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 870
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.682e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.4e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 5.669999999999999e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 7.02e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.15e0

QD
type: SiteQuality
SIO_000300: 1.262e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.47e-1

FS
type: SiteQuality
SIO_000300: 6.44e-1

DP
type: SiteQuality
SIO_000300: 1.46926e6

MQRankSum
type: SiteQuality
SIO_000300: 6.19e-1

GenotypeDepth
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bin: 2.75e1
variant carriers: 1

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 12

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 399
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variant carriers: 0

GenotypeQuality
all individuals: 58
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1064
bin: 4.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 123
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 417
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 113
bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 941
bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 293
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 771
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1744
bin: 3.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6404
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9912
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63990
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 868
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11328
num of homozygotes: 0

South Asian
type: Population
allele count: 12
allele frequency: 7.44324525493115e-4
allele num: 16122
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8482
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.467732e6

MQRankSum
type: SiteQuality
SIO_000300: 4.17e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.13e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.4e-3

QD
type: SiteQuality
SIO_000300: 1.24e1

FS
type: SiteQuality
SIO_000300: 1.489e0

MQ
type: SiteQuality
SIO_000300: 5.627e1

VQSLOD
type: SiteQuality
SIO_000300: -7.644e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.43e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.0e-2

GenotypeDepth
all individuals: 6
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 627
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 34891
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 108
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 395
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variant carriers: 0

GenotypeQuality
all individuals: 1793
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 781
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variant carriers: 0

GenotypeQuality
all individuals: 4251
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variant carriers: 0

GenotypeQuality
all individuals: 1997
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 41
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variant carriers: 0

GenotypeQuality
all individuals: 770
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 293
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 101
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 421
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variant carriers: 0

GenotypeQuality
all individuals: 6661
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1911
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1693
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 884
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1038
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1747
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 272
bin: 8.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 872
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6400
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11336
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.561572816140417e-5
allele num: 64038
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8488
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9924
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16120
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.182e1

FS
type: SiteQuality
SIO_000300: 7.05e-1

VQSLOD
type: SiteQuality
SIO_000300: -8.891e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.68e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.082e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.4e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -1.7e0

MQ
type: SiteQuality
SIO_000300: 5.635e1

MQRankSum
type: SiteQuality
SIO_000300: 3.34e-1

DP
type: SiteQuality
SIO_000300: 1.46451e6

GenotypeDepth
all individuals: 3
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variant carriers: 0

GenotypeQuality
all individuals: 1747
bin: 3.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 2

GenotypeQuality
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GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1693
bin: 7.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9924
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16120
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8488
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.764290755116443e-4
allele num: 11336
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64038
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 872
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6400
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.7e0

FS
type: SiteQuality
SIO_000300: 7.05e-1

VQSLOD
type: SiteQuality
SIO_000300: -8.891e-1

MQ
type: SiteQuality
SIO_000300: 5.635e1

MQRankSum
type: SiteQuality
SIO_000300: 3.34e-1

QD
type: SiteQuality
SIO_000300: 1.182e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.4e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -1.082e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.68e-1

DP
type: SiteQuality
SIO_000300: 1.46451e6

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 34636
bin: 6.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16104
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9918
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64022
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8480
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.833922261484099e-5
allele num: 11320
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6388
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 870
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -2.83e-1

VQSLOD
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ClippingRankSum
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SIO_000300: 1.05e0

BaseQRankSum
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FS
type: SiteQuality
SIO_000300: 1.657e0

DP
type: SiteQuality
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QD
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.477e1

InbreedingCoeff
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SIO_000300: -8.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.89e-1

GenotypeDepth
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 953
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GenotypeQuality
all individuals: 1149
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GenotypeQuality
all individuals: 383
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GenotypeQuality
all individuals: 1840
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GenotypeQuality
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GenotypeQuality
all individuals: 830
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GenotypeQuality
all individuals: 1605
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GenotypeQuality
all individuals: 757
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variant carriers: 0

GenotypeQuality
all individuals: 288
bin: 9.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 870
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.562793023691942e-5
allele num: 63988
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11334
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16062
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9924
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8488
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6402
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.808e1

VQSLOD
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SIO_000300: -1.67e0

MQ
type: SiteQuality
SIO_000300: 5.699e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -4.82e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.272e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.01e0

DP
type: SiteQuality
SIO_000300: 1.454916e6

ClippingRankSum
type: SiteQuality
SIO_000300: 1.36e0

GenotypeDepth
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 2.5e0
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 5.25e1
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GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 3.25e1
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GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4436
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 624
bin: 9.75e1
variant carriers: 2

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63956
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6402
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11328
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16054
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 866
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8488
num of homozygotes: 0

African
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allele frequency: 2.016129032258065e-4
allele num: 9920
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.084e0

FS
type: SiteQuality
SIO_000300: 3.313e0

InbreedingCoeff
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SIO_000300: -8.0e-4

ReadPosRankSum
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BaseQRankSum
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MQ
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SIO_000300: 5.667e1

DP
type: SiteQuality
SIO_000300: 1.44989e6

ClippingRankSum
type: SiteQuality
SIO_000300: -3.46e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.22e-1

QD
type: SiteQuality
SIO_000300: 1.446e1

GenotypeDepth
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variant carriers: 0

GenotypeQuality
all individuals: 1575
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 3

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 33490
bin: 6.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9916
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 866
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 63892
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6396
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16030
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11326
num of homozygotes: 0

East Asian
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allele count: 3
allele frequency: 3.533568904593639e-4
allele num: 8490
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.0e-4

VQSLOD
type: SiteQuality
SIO_000300: -1.302e0

FS
type: SiteQuality
SIO_000300: 6.25e-1

QD
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BaseQRankSum
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SIO_000300: -2.683e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.57e-1

DP
type: SiteQuality
SIO_000300: 1.444587e6

MQRankSum
type: SiteQuality
SIO_000300: -4.07e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.026e0

MQ
type: SiteQuality
SIO_000300: 5.743e1

GenotypeDepth
all individuals: 54
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4567
bin: 2.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 283
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variant carriers: 0

GenotypeQuality
all individuals: 2376
bin: 3.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6366
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9898
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15950
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11296
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 862
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8468
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.567545537197856e-5
allele num: 63794
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.96e0

BaseQRankSum
type: SiteQuality
SIO_000300: -7.81e-1

FS
type: SiteQuality
SIO_000300: 4.527e0

MQRankSum
type: SiteQuality
SIO_000300: -2.2e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.9e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.24e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.4e-3

DP
type: SiteQuality
SIO_000300: 1.435573e6

QD
type: SiteQuality
SIO_000300: 9.140000000000001e0

MQ
type: SiteQuality
SIO_000300: 5.728e1

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1209
bin: 5.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11296
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8468
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9898
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15950
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6366
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.567545537197856e-5
allele num: 63794
num of homozygotes: 0

Other
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ClippingRankSum
type: SiteQuality
SIO_000300: -1.24e-1

FS
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InbreedingCoeff
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MQ
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VQSLOD
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ReadPosRankSum
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BaseQRankSum
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MQRankSum
type: SiteQuality
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QD
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DP
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SIO_000300: 1.435573e6

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 3.25e1
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GenotypeQuality
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GenotypeQuality
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bin: 5.25e1
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GenotypeQuality
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bin: 6.25e1
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GenotypeQuality
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bin: 8.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6366
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.269592476489028e-5
allele num: 15950
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11296
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8468
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63794
num of homozygotes: 0

African
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allele frequency: 0.0e0
allele num: 9898
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
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VQSLOD
type: SiteQuality
SIO_000300: 1.96e0

MQRankSum
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InbreedingCoeff
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ClippingRankSum
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QD
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MQ
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FS
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DP
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ReadPosRankSum
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BaseQRankSum
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GenotypeDepth
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 4

GenotypeQuality
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GenotypeQuality
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bin: 6.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6386
num of homozygotes: 0

South Asian
type: Population
allele count: 4
allele frequency: 2.515723270440251e-4
allele num: 15900
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

Latino
type: Population
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Other
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East Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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MQRankSum
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MQ
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QD
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VQSLOD
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BaseQRankSum
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FS
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ClippingRankSum
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InbreedingCoeff
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DP
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ReadPosRankSum
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 1586
bin: 5.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11292
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8470
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.01461038961039e-4
allele num: 9856
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6382
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 63666
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Other
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South Asian
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allele frequency: 0.0e0
allele num: 15856
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -2.226e0

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -8.65e-1

MQ
type: SiteQuality
SIO_000300: 5.82e1

DP
type: SiteQuality
SIO_000300: 1.420659e6

QD
type: SiteQuality
SIO_000300: 7.29e0

MQRankSum
type: SiteQuality
SIO_000300: 1.52e0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.56e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.11e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.6e-3

GenotypeDepth
all individuals: 14
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4884
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 610
bin: 9.75e1
variant carriers: 8

GenotypeQuality
all individuals: 2566
bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1604
bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 400
bin: 7.5e0
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 31548
bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5878
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 705
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1124
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1652
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 275
bin: 9.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9860
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6378
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 6
allele frequency: 9.419743782969103e-5
allele num: 63696
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11302
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 864
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.262785705265816e-4
allele num: 15838
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8478
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -3.08e-1

FS
type: SiteQuality
SIO_000300: 4.24e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.108e0

QD
type: SiteQuality
SIO_000300: 1.241e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.53e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.667e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.6e-2

MQ
type: SiteQuality
SIO_000300: 5.811e1

DP
type: SiteQuality
SIO_000300: 1.417088e6

GenotypeDepth
all individuals: 14
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2537
bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5873
bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 1440
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 703
bin: 8.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9866
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6378
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.17813383600377e-4
allele num: 8488
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 858
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11306
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.569710859259724e-5
allele num: 63706
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15844
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.777e1

MQRankSum
type: SiteQuality
SIO_000300: 4.11e-1

FS
type: SiteQuality
SIO_000300: 9.771000000000001e0

DP
type: SiteQuality
SIO_000300: 1.417431e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.34e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.267e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.878e0

QD
type: SiteQuality
SIO_000300: 1.607e1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.01e-1

GenotypeDepth
all individuals: 6
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 22
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 130
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 377
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variant carriers: 0

GenotypeQuality
all individuals: 5472
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variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 600
bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1512
bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1376
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1321
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 31913
bin: 6.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 852
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6370
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9856
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15596
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8478
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11294
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.571338780641106e-5
allele num: 63640
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 3.45e-1

MQ
type: SiteQuality
SIO_000300: 5.879e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.16e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.642e0

VQSLOD
type: SiteQuality
SIO_000300: -1.305e0

QD
type: SiteQuality
SIO_000300: 7.69e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.1e-2

DP
type: SiteQuality
SIO_000300: 1.392082e6

FS
type: SiteQuality
SIO_000300: 1.451e0

GenotypeDepth
all individuals: 3
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7146
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 28
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 601
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 32174
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1623
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variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1311
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 262
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variant carriers: 0

GenotypeQuality
all individuals: 387
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variant carriers: 0

GenotypeQuality
all individuals: 5386
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1493
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 130
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5337
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2527
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 668
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variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1262
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2889
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2546
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1177
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 473
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 258
bin: 8.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8482
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 852
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6366
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.143171460003143e-5
allele num: 63630
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9862
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11278
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15548
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.56e0

FS
type: SiteQuality
SIO_000300: 3.451e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.94e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-4

QD
type: SiteQuality
SIO_000300: 1.029e1

VQSLOD
type: SiteQuality
SIO_000300: -1.729e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.52e-1

MQ
type: SiteQuality
SIO_000300: 5.785e1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.45e-1

DP
type: SiteQuality
SIO_000300: 1.388405e6

GenotypeDepth
all individuals: 75
bin: 5.25e1
variant carriers: 1

GenotypeDepth
all individuals: 6
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variant carriers: 0

GenotypeDepth
all individuals: 3
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variant carriers: 0

GenotypeQuality
all individuals: 5287
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variant carriers: 0

GenotypeQuality
all individuals: 3025
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variant carriers: 0

GenotypeQuality
all individuals: 317
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GenotypeQuality
all individuals: 650
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variant carriers: 57

GenotypeQuality
all individuals: 1839
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variant carriers: 0

GenotypeQuality
all individuals: 69
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GenotypeQuality
all individuals: 2839
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 263
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GenotypeQuality
all individuals: 680
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GenotypeQuality
all individuals: 262
bin: 9.25e1
variant carriers: 1

GenotypeQuality
all individuals: 429
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2723
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1480
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variant carriers: 0

GenotypeQuality
all individuals: 1601
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 678
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variant carriers: 0

GenotypeQuality
all individuals: 2168
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variant carriers: 0

GenotypeQuality
all individuals: 5272
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 29574
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variant carriers: 0

GenotypeQuality
all individuals: 1320
bin: 7.75e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.522306287503261e-5
allele num: 15332
num of homozygotes: 0

East Asian
type: Population
allele count: 25
allele frequency: 2.95159386068477e-3
allele num: 8470
num of homozygotes: 1

Other
type: Population
allele count: 2
allele frequency: 2.352941176470588e-3
allele num: 850
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 5
allele frequency: 7.883948281299275e-4
allele num: 6342
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11278
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 26
allele frequency: 4.104831070413641e-4
allele num: 63340
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9760
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.785e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.4e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 3.06e-1

MQRankSum
type: SiteQuality
SIO_000300: 5.12e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.99e-1

DP
type: SiteQuality
SIO_000300: 1.379452e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.97e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.6e-2

MQ
type: SiteQuality
SIO_000300: 5.846e1

QD
type: SiteQuality
SIO_000300: 1.444e1

GenotypeDepth
all individuals: 33
bin: 6.25e1
variant carriers: 3

GenotypeDepth
all individuals: 5
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variant carriers: 0

GenotypeDepth
all individuals: 24
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variant carriers: 1

GenotypeQuality
all individuals: 1570
bin: 1.75e1
variant carriers: 7

GenotypeQuality
all individuals: 88
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variant carriers: 2

GenotypeQuality
all individuals: 2747
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GenotypeQuality
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variant carriers: 13

GenotypeQuality
all individuals: 22079
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variant carriers: 6

GenotypeQuality
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bin: 4.25e1
variant carriers: 14

GenotypeQuality
all individuals: 2486
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GenotypeQuality
all individuals: 316
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variant carriers: 16

GenotypeQuality
all individuals: 1100
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variant carriers: 3

GenotypeQuality
all individuals: 3453
bin: 4.75e1
variant carriers: 10

GenotypeQuality
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bin: 3.75e1
variant carriers: 14

GenotypeQuality
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variant carriers: 2

GenotypeQuality
all individuals: 3458
bin: 3.25e1
variant carriers: 9

GenotypeQuality
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bin: 2.25e1
variant carriers: 11

GenotypeQuality
all individuals: 1168
bin: 1.25e1
variant carriers: 8

GenotypeQuality
all individuals: 2927
bin: 6.75e1
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GenotypeQuality
all individuals: 656
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GenotypeQuality
all individuals: 99
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GenotypeQuality
all individuals: 3574
bin: 5.25e1
variant carriers: 7

GenotypeQuality
all individuals: 241
bin: 8.25e1
variant carriers: 1

Latino
type: Population
allele count: 1
allele frequency: 9.33184023889511e-5
allele num: 10716
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 94
allele frequency: 1.644794400699912e-3
allele num: 57150
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 746
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.98909700866648e-5
allele num: 14308
num of homozygotes: 0

African
type: Population
allele count: 14
allele frequency: 1.573387278040009e-3
allele num: 8898
num of homozygotes: 0

East Asian
type: Population
allele count: 4
allele frequency: 4.951720722951226e-4
allele num: 8078
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 8
allele frequency: 1.466813348001467e-3
allele num: 5454
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 2.18615e2

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.39e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.12e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.176e2

ClippingRankSum
type: SiteQuality
SIO_000300: 5.5e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.163e0

QD
type: SiteQuality
SIO_000300: 8.5e-1

MQRankSum
type: SiteQuality
SIO_000300: -6.4e-2

DP
type: SiteQuality
SIO_000300: 1.373855e6

MQ
type: SiteQuality
SIO_000300: 5.838e1

GenotypeDepth
all individuals: 5171
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 603
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variant carriers: 0

GenotypeDepth
all individuals: 10
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variant carriers: 0

GenotypeQuality
all individuals: 1977
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variant carriers: 0

GenotypeQuality
all individuals: 1368
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GenotypeQuality
all individuals: 989
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GenotypeQuality
all individuals: 540
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variant carriers: 0

GenotypeQuality
all individuals: 128
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GenotypeQuality
all individuals: 5306
bin: 6.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 2213
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variant carriers: 0

GenotypeQuality
all individuals: 360
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GenotypeQuality
all individuals: 430
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GenotypeQuality
all individuals: 1207
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GenotypeQuality
all individuals: 1066
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GenotypeQuality
all individuals: 4781
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variant carriers: 0

GenotypeQuality
all individuals: 56
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GenotypeQuality
all individuals: 36429
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GenotypeQuality
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GenotypeQuality
all individuals: 1003
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GenotypeQuality
all individuals: 350
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GenotypeQuality
all individuals: 141
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GenotypeQuality
all individuals: 133
bin: 9.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15188
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8490
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.571338780641106e-5
allele num: 63640
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11310
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9808
num of homozygotes: 0

Other
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allele count: 0
allele frequency: 0.0e0
allele num: 854
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.08e-1

QD
type: SiteQuality
SIO_000300: 1.053e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.88e-1

DP
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SIO_000300: 1.409187e6

InbreedingCoeff
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SIO_000300: -4.0e-4

BaseQRankSum
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SIO_000300: -3.799e0

FS
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SIO_000300: 0.0e0

MQRankSum
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SIO_000300: 1.06e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 4.15e-1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 6.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8504
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6372
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9838
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11304
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 858
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15152
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.569021244547651e-5
allele num: 63734
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.09e-1

BaseQRankSum
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SIO_000300: -3.12e-1

ClippingRankSum
type: SiteQuality
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FS
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MQ
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SIO_000300: 5.899e1

VQSLOD
type: SiteQuality
SIO_000300: 4.5e-1

MQRankSum
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SIO_000300: 3.12e-1

QD
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SIO_000300: 1.504e1

DP
type: SiteQuality
SIO_000300: 1.420464e6

GenotypeDepth
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variant carriers: 1

GenotypeDepth
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variant carriers: 5

GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 332

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

South Asian
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allele count: 1
allele frequency: 6.622516556291391e-5
allele num: 15100
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8512
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.70425892241109e-5
allele num: 63772
num of homozygotes: 0

African
type: Population
allele count: 311
allele frequency: 3.15160113498176e-2
allele num: 9868
num of homozygotes: 5

Latino
type: Population
allele count: 25
allele frequency: 2.211997876482039e-3
allele num: 11302
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 856
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6376
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 3.11e-1

MQ
type: SiteQuality
SIO_000300: 5.86e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.92e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.05e-1

DP
type: SiteQuality
SIO_000300: 1.431571e6

BaseQRankSum
type: SiteQuality
SIO_000300: 1.23e0

ClippingRankSum
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SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.368e1

VQSLOD
type: SiteQuality
SIO_000300: 1.17e0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 4

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 773
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GenotypeQuality
all individuals: 803
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variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9886
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 6.255473539346929e-5
allele num: 63944
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15058
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11322
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6400
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 860
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8524
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -9.9e-2

MQ
type: SiteQuality
SIO_000300: 5.877e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.21e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.5e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.47e-1

FS
type: SiteQuality
SIO_000300: 2.285e0

VQSLOD
type: SiteQuality
SIO_000300: -4.877e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.59e-1

DP
type: SiteQuality
SIO_000300: 1.438712e6

QD
type: SiteQuality
SIO_000300: 1.145e1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 1042
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variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9876
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8530
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11336
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6396
num of homozygotes: 0

Other
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allele count: 0
allele frequency: 0.0e0
allele num: 856
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14938
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.562109472631842e-5
allele num: 64016
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.72e-1

MQ
type: SiteQuality
SIO_000300: 5.801e1

InbreedingCoeff
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SIO_000300: -1.1e-3

DP
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ReadPosRankSum
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FS
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BaseQRankSum
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VQSLOD
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QD
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MQRankSum
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8552
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11350
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

African
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allele count: 3
allele frequency: 3.03275374039628e-4
allele num: 9892
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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South Asian
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allele frequency: 0.0e0
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num of homozygotes: 0

Other
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InbreedingCoeff
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MQ
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MQRankSum
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ReadPosRankSum
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BaseQRankSum
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FS
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QD
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VQSLOD
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ClippingRankSum
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DP
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 5

Latino
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num of homozygotes: 0

African
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European (Finnish)
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South Asian
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Other
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European (Non-Finnish)
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allele frequency: 0.0e0
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East Asian
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ClippingRankSum
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ReadPosRankSum
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MQ
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FS
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VQSLOD
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InbreedingCoeff
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MQRankSum
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BaseQRankSum
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DP
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QD
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8570
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.799020940984498e-5
allele num: 14708
num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
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num of homozygotes: 0

African
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allele frequency: 1.01010101010101e-4
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Other
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num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 1.56162158785683e-5
allele num: 64036
num of homozygotes: 0

DP
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MQ
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MQRankSum
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QD
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ClippingRankSum
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VQSLOD
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FS
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ReadPosRankSum
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InbreedingCoeff
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BaseQRankSum
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GenotypeDepth
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variant carriers: 1

GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Finnish)
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East Asian
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South Asian
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Other
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African
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allele frequency: 1.01010101010101e-4
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European (Non-Finnish)
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ClippingRankSum
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VQSLOD
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MQ
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InbreedingCoeff
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FS
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QD
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BaseQRankSum
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DP
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ReadPosRankSum
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MQRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 64072
num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
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Latino
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num of homozygotes: 0

African
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European (Finnish)
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Other
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South Asian
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FS
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MQ
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MQRankSum
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ReadPosRankSum
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InbreedingCoeff
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BaseQRankSum
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QD
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VQSLOD
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ClippingRankSum
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DP
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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allele count: 0
allele frequency: 0.0e0
allele num: 852
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.951202558042541e-5
allele num: 14386
num of homozygotes: 0

African
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allele frequency: 0.0e0
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East Asian
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allele count: 0
allele frequency: 0.0e0
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European (Finnish)
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allele count: 1
allele frequency: 1.557632398753894e-4
allele num: 6420
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 64058
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Latino
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allele frequency: 0.0e0
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ClippingRankSum
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SIO_000300: 1.43e0

MQ
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SIO_000300: 5.901e1

FS
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MQRankSum
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VQSLOD
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QD
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InbreedingCoeff
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DP
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SIO_000300: 1.460223e6

ReadPosRankSum
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SIO_000300: -1.03e0

BaseQRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

South Asian
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allele count: 2
allele frequency: 1.393922497909116e-4
allele num: 14348
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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African
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Other
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European (Non-Finnish)
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allele num: 64046
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European (Finnish)
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East Asian
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FS
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ClippingRankSum
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ReadPosRankSum
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InbreedingCoeff
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MQRankSum
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VQSLOD
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MQ
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BaseQRankSum
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QD
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DP
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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allele count: 0
allele frequency: 0.0e0
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East Asian
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South Asian
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Other
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele num: 63812
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Latino
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European (Finnish)
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MQRankSum
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FS
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QD
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BaseQRankSum
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ReadPosRankSum
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DP
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InbreedingCoeff
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MQ
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VQSLOD
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ClippingRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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allele count: 0
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Latino
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African
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Other
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European (Finnish)
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European (Non-Finnish)
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East Asian
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FS
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DP
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InbreedingCoeff
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ReadPosRankSum
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MQRankSum
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ClippingRankSum
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VQSLOD
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QD
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MQ
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BaseQRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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allele frequency: 0.0e0
allele num: 846
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6426
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 14046
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8578
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9910
num of homozygotes: 0

Latino
type: Population
allele count: 4
allele frequency: 3.512469265893923e-4
allele num: 11388
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.564994209521425e-5
allele num: 63898
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.889e1

QD
type: SiteQuality
SIO_000300: 9.710000000000001e0

VQSLOD
type: SiteQuality
SIO_000300: 1.39e-1

FS
type: SiteQuality
SIO_000300: 5.26e-1

MQRankSum
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SIO_000300: 4.96e-1

DP
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SIO_000300: 1.461081e6

InbreedingCoeff
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SIO_000300: 3.4e-3

ClippingRankSum
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SIO_000300: -5.27e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.55e-1

BaseQRankSum
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SIO_000300: -1.366e0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 121
bin: 8.75e1
variant carriers: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9910
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6426
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 14046
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8578
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11388
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 846
num of homozygotes: 0

European (Non-Finnish)
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allele count: 2
allele frequency: 3.129988419042849e-5
allele num: 63898
num of homozygotes: 0

ReadPosRankSum
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SIO_000300: 4.55e-1

DP
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SIO_000300: 1.461081e6

MQRankSum
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SIO_000300: 4.96e-1

InbreedingCoeff
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SIO_000300: 3.4e-3

BaseQRankSum
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SIO_000300: -1.366e0

ClippingRankSum
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SIO_000300: -5.27e-1

FS
type: SiteQuality
SIO_000300: 5.26e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.39e-1

QD
type: SiteQuality
SIO_000300: 9.710000000000001e0

MQ
type: SiteQuality
SIO_000300: 5.889e1

GenotypeDepth
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variant carriers: 1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 312
bin: 9.75e1
variant carriers: 6

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.134599711616826e-5
allele num: 63804
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 7.150007150007151e-5
allele num: 13986
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 840
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

European (Finnish)
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allele count: 3
allele frequency: 4.664179104477612e-4
allele num: 6432
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8576
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9900
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 5.53e-1

ClippingRankSum
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SIO_000300: 2.11e-1

MQRankSum
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SIO_000300: 4.86e-1

DP
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SIO_000300: 1.458257e6

QD
type: SiteQuality
SIO_000300: 9.859999999999999e0

ReadPosRankSum
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SIO_000300: 2.84e-1

MQ
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SIO_000300: 5.914e1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
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SIO_000300: -4.7e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.9e-3

GenotypeDepth
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bin: 9.75e1
variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 840
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6432
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.134599711616826e-5
allele num: 63804
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9900
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8576
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11376
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.914e1

DP
type: SiteQuality
SIO_000300: 1.458257e6

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
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SIO_000300: 5.53e-1

MQRankSum
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SIO_000300: 4.86e-1

BaseQRankSum
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SIO_000300: -4.7e-1

ClippingRankSum
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SIO_000300: 2.11e-1

QD
type: SiteQuality
SIO_000300: 9.859999999999999e0

InbreedingCoeff
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SIO_000300: 1.9e-3

ReadPosRankSum
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SIO_000300: 2.84e-1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 832
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.759943681802182e-4
allele num: 11364
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9844
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
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South Asian
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 2.325e0

InbreedingCoeff
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VQSLOD
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ClippingRankSum
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BaseQRankSum
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ReadPosRankSum
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MQRankSum
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DP
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SIO_000300: 1.449276e6

MQ
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SIO_000300: 5.925e1

QD
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SIO_000300: 7.39e0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 2.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9844
num of homozygotes: 0

South Asian
type: Population
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allele frequency: 0.0e0
allele num: 13546
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11364
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6428
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.16795141322121e-4
allele num: 8562
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63498
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 2.325e0

MQ
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ClippingRankSum
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InbreedingCoeff
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ReadPosRankSum
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BaseQRankSum
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MQRankSum
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VQSLOD
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DP
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QD
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

Other
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

Latino
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allele count: 0
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num of homozygotes: 0

South Asian
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African
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allele count: 0
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East Asian
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FS
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MQRankSum
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InbreedingCoeff
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VQSLOD
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MQ
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DP
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ClippingRankSum
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BaseQRankSum
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ReadPosRankSum
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QD
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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